Biosynthetic genes for spinosyn insecticide production

ABSTRACT

Spinosyn biosynthetic genes, spinosyn producing microorganisms transformed with the biosynthetic genes, methods using the biosynthetic genes to increase production of spinosyn insecticidal macrolides, and methods using the genes or fragments thereof to change the products produced by spinosyn-producing microorganisms.

SUMMARY OF THE INVENTION

[0001] The present invention provides novel biosynthetic genes, vectors incorporating the biosynthetic genes, Saccharopolyspora spinosa strains transformed with the biosynthetic genes, methods using these genes to increase production of spinosyn insecticidal macrolides, and methods using the genes or fragments thereof to change the products produced by spinosyn-producing strains of Saccharopolyspora spinosa.

BACKGROUND OF THE INVENTION

[0002] As disclosed in U.S. Pat. No. 5,362,634, fermentation product A83543 is a family of related compounds produced by Saccharopolyspora spinosa. The known members of this family have been referred to as factors or components, and each has been given an identifying letter designation. These compounds are hereinafter referred to as spinosyn A, B, etc. The spinosyn compounds are useful for the control of arachnids, nematodes and insects, in particular Lepidoptera and Diptera species, and they are quite environmentally friendly and have an appealing toxicological profile. Tables 1 and 2 identify the structures of a variety of known spinosyn compounds: TABLE 1

Factor R^(1′) R^(2′) R^(3′) R^(4′) R^(5′) R^(6′) R^(7′) spinosyn A H CH₃

C₂H₅ CH₃ CH₃ CH₃ (a) spinosyn B H CH₃

C₂H₅ CH₃ CH₃ CH₃ (b) spinosyn C H CH₃

C₂H₅ CH₃ CH₃ CH₃ (c) spinosyn D CH₃ CH₃ (a) C₂H₅ CH₃ CH₃ CH₃ spinosyn E H CH₃ (a) CH₃ CH₃ CH₃ CH₃ spinosyn F H H (a) C₂H₅ CH₃ CH₃ CH₃ spinosyn G H CH₃

C₂H₅ CH₃ CH₃ CH₃ (d) spinosyn H H CH₃ (a) C₂H₅ H CH₃ CH₃ spinosyn J H CH₃ (a) C₂H₅ CH₃ H CH₃ spinosyn K H CH₃ (a) C₂H₅ CH₃ CH₃ H spinosyn L CH₃ CH₃ (a) C₂H₅ CH₃ H CH₃ spinosyn M H CH₃ (b) C₂H₅ CH₃ H CH₃ spinosyn N CH₃ CH₃ (b) C₂H₅ CH₃ H CH₃ spinosyn O CH₃ CH₃ (a) C₂H₅ CH₃ CH₃ H spinosyn P H CH₃ (a) C₂H₅ CH₃ H H spinosyn Q CH₃ CH₃ (a) C₂H₅ H CH₃ CH₃ spinosyn R H CH₃ (b) C₂H₅ H CH₃ CH₃ spinosyn S H CH₃ (a) CH₃ H CH₃ CH₃ spinosyn T H CH₃ (a) C₂H₅ H H CH₃ spinosyn U H CH₃ (a) C₂H₅ H CH₃ H spinosyn V CH₃ CH₃ (a) C₂H₅ H CH₃ H spinosyn W CH₃ CH₃ (a) C₂H₅ CH₃ H H spinosyn Y H CH₃ (a) CH₃ CH₃ CH₃ H spinosyn A 17- H CH₃ H C₂H₅ CH₃ CH₃ CH₃ Psa spinosyn D 17- CH₃ CH₃ H C₂H₅ CH₃ CH₃ CH₃ Psa spinosyn E 17- H CH₃ H CH₃ CH₃ CH₃ CH₃ Psa spinosyn F 17- H H H C₂H₅ CH₃ CH₃ CH₃ Psa spinosyn H 17- H CH₃ H C₂H₅ H CH₃ CH₃ Psa spinosyn J 17- H CH₃ H C₂H₅ CH₃ H CH₃ Psa spinosyn L 17- CH₃ CH₃ H C₂H₅ CH₃ H CH₃ Psa

[0003] TABLE 2

Factor R^(1′) R^(2′) R^(3′) R^(4′) R^(5′) spinosyn A 9-Psa H CH₃

C₂H₅ H (a) spinosyn D 9-Psa CH₃ CH₃ (a) C₂H₅ H spinosyn A H CH₃ H C₂H₅ H Aglycone spinosyn D CH₃ CH₃ H C₂H₅ H Aglycone

[0004] The naturally produced spinosyn compounds consist of a 5,6,5-tricylic ring system, fused to a 12-membered macrocyclic lactone, a neutral sugar (rhamnose) and an amino sugar (forosamine) (see Kirst et al. (1991). If the amino sugar is not present the compounds have been referred to as the pseudoaglycone of A, D, etc., and if the neutral sugar is not present then the compounds have been referred to as the reverse pseudoaglycone of A, D, etc. A more preferred nomenclature is to refer to the pseudoaglycones as spinosyn A 17-Psa, spinosyn D 17-Psa, etc., and to the reverse pseudoaglycones as spinosyn A 9-Psa, spinosyn D 9-Psa, etc.

[0005] The naturally produced spinosyn compounds may be produced via fermentation from cultures NRRL 18395, 18537, 18538, 18539, 18719, 18720, 18743 and 18823. These cultures have been deposited and made part of the stock culture collection of the Midwest Area Northern Regional Research Center, Agricultural Research Service, United States Department of Agriculture, 1815 North University Street, Peoria, Ill. 61604.

[0006] U.S. Pat. No. 5,362,634 and corresponding European Patent Application No. 375316 A1 disclose spinosyns A, B, C, D, E, F, G, H, and J. These compounds are disclosed as being produced by culturing a strain of the novel microorganism Saccharopolyspora spinosa selected from NRRL 18395, NRRL 18537, NRRL 18538, and NRRL 18539.

[0007] WO 93/09126 disclosed spinosyns L, M, N, Q, R, S, and T. Also disclosed therein are two spinosyn J producing strains: NRRL 18719 and NRRL 18720, and a strain that produces spinosyns Q, R, S, and T: NRRL 18823.

[0008] WO 94/20518 and U.S. Pat. No. 5,6704,486 disclose spinosyns K, O, P, U, V, W, and Y, and derivatives thereof. Also disclosed is spinosyn K-producing strain NRRL 18743.

[0009] A challenge in producing spinosyn compounds arises from the fact that a very large fermentation volume is required to produce a very small quantity of spinosyns. It is highly desired to increase spinosyn production efficiency and thereby increase availability of the spinosyns while reducing their cost. A cloned fragment of DNA containing genes for spinosyn biosynthetic enzymes would enable duplication of genes coding for rate limiting enzymes in the production of spinosyns. This could be used to increase yield in any circumstance when one of the encoded activities limited synthesis of the desired spinosyn. A yield increase of this type was achieved in fermentations of Streptomyces fradiae by duplicating the gene encoding a rate-limiting methyltransferase that converts macrocin to tylosin (Baltz et al., 1997).

[0010] Cloned biosynthetic genes would also provide a method for producing new derivatives of the spinosyns which may have a different spectrum of insecticidal activity. New derivatives are desirable because, although known spinosyns inhibit a broad spectrum of insects, they do not control all pests. Different patterns of control may be provided by biosynthetic intermediates of the spinosyns, or by their derivatives produced in vivo, or by derivatives resulting from their chemical modification in vitro. Specific intermediates (or their natural derivatives) could be synthesized by mutant strains of S. spinosa in which certain genes encoding enzymes for spinosyn biosynthesis have been disrupted. Such strains can be generated by integrating, via homologous recombination, a mutagenic plasmid containing an internal fragment of the target gene. Upon plasmid integration, two incomplete copies of the biosynthetic gene are formed, thereby eliminating the enzymatic function it encoded. The substrate for this enzyme, or some natural derivative thereof, should accumulate upon fermentation of the mutant strain. Such a strategy was used effectively to generate a strain of Saccharopolyspora erythraea producing novel 6-deoxyerythromycin derivatives (Weber & McAlpine, 1992).

[0011] Novel intermediates could also be synthesized by mutant strains of S. spinosa in which parts of certain genes encoding enzymes for spinosyn biosynthesis have been replaced with parts of the same gene which have been specifically mutated in vitro, or with corresponding parts of genes from other organisms. Such strains could be generated by swapping the target region, via double homologous recombination, with a mutagenic plasmid containing the new fragment between non-mutated sequences which flank the target region. The hybrid gene would produce protein with altered functions, either lacking an activity or performing a novel enzymatic transformation. A new derivative would accumulate upon fermentation of the mutant strain. Such a strategy was used to generate a strain of Saccharopolyspora erythraea producing a novel anhydroerythromycin derivative (Donadio et al., 1993).

[0012] Biosynthesis of spinosyns proceeds via stepwise condensation and modification of 2- and 3-carbon carboxylic acid precursors, generating a linear polyketide that is cyclized and bridged to produce the tetracyclic aglycone. Pseudoaglycone (containing tri-O-methylated rhamnose) is formed next, then di-N-methylated forosamine is added to complete the biosynthesis (Broughton et al., 1991). Other macrolides, such as the antibiotic erythromycin, the antiparasitic avermectin and the immunosuppressant rapamycin, are synthesized in a similar fashion. In the bacteria producing these compounds, most of the macrolide biosynthetic genes are clustered together in a 70-80 kb region of the genome (Donadio et al., 1991; MacNeil et al., 1992; Schwecke et al., 1995). At the centers of these clusters are 3-5 highly conserved genes coding for the very large, multifunctional proteins of a Type I polyketide synthase (PKS). Together the polypeptides form a complex consisting of an initiator module and several extender modules, each of which adds a specific acyl-CoA precursor to a growing polyketide chain, and modifies the β-keto group in a specific manner. The structure of a polyketide is therefore determined by the composition and order of the modules in the PKS. A module comprises several domains, each of which performs a specific function. The initiator module consists of an acyl transferase (AT) domain for addition of the acyl group from the precursor to an acyl carrier protein (ACP) domain. The extender modules contain these domains, along with a β-ketosynthase (KS) domain that adds the pre-existing polyketide chain to the new acyl-ACP by decarboxylative condensation. Additional domains may also be present in the extender modules to carry out specific β-keto modifications: a β-ketoreductase (KR) domain to reduce the β-keto group to a hydroxyl group, a dehydratase (DH) domain to remove the hydroxyl group and leave a double bond, and an enoyl reductase (ER) domain to reduce the double bond and leave a saturated carbon. The last extender module terminates with a thioesterase (TE) domain that liberates the polyketide from the PKS enzyme in the form of a macrocyclic lactone.

[0013] Macrolides are derived from macrocyclic lactones by additional modifications, such as methylation and changes in reductive state, and the addition of unusual sugars. Most of the genes required for these modifications, and for the synthesis and attachment of the sugars, are clustered around the PKS genes. The genes encoding deoxysugar biosynthetic enzymes are similar in producers of macrolide antibiotics, such as erythromycin and tylosin (Donadio et al., 1993; Merson-Davies & Cundliffe, 1994), and producers of extracellular polysaccharides, such as the O-antigens of Salmonella and Yersinia (Jiang et al., 1991; Kessler et al., 1993). All these syntheses involve activation of glucose by the addition of a nucleotide diphosphate, followed by dehydration, reduction and/or epimerization. The resultant sugar could undergo one or more modifications such as deoxygenation, transamination and methylation, depending upon the type of sugar moiety present in the macrolide. The sugars are incorporated into macrolides by the action of specific glycosyltransferases. Genes involved in the synthesis and attachment of a sugar may be tightly clustered—even transcribed as a single operon—or they may be dispersed (Decker & Hutchinson, 1993; Jarvis & Hutchinson, 1994). Spinosyn synthesis also involves bridging of the lactone nucleus, an activity that is rare in macrolide producers. Therefore, the spinosyn biosynthetic cluster may uniquely contain additional genes encoding enzymes for this function.

[0014] The following terms are used herein as defined below:

[0015] AniR—the apramycin resistance-conferring gene.

[0016] ApR—the ampicillin resistance-conferring gene.

[0017] ACP—acyl carrier protein.

[0018] AT—acyltransferase.

[0019] bp—base pairs.

[0020] Cloning—the process of incorporating a segment of DNA into a recombinant DNA cloning vector and transforming a host cell with the recombinant DNA.

[0021] CmR—the chloramphenicol resistance-conferring gene.

[0022] Codon bias—the propensity to use a particular codon to specify a specific amino acid. In the case of S. spinosa, the propensity is to use a codon having cytosine or guanine as the third base.

[0023] Complementation—the restoration of a mutant strain to its normal phenotype by a cloned gene.

[0024] Conjugation—a process in which genetic material is transferred from one bacterial cell to another.

[0025] cos—the lambda cohesive end sequence.

[0026] Cosmid—a recombinant DNA cloning vector which is a plasmid that not only can replicate in a host cell in the same manner as a plasmid but also can be packaged into phage heads.

[0027] DH—dehydratase.

[0028] ER—enoyl reductase.

[0029] Exconjugant—recombinant strain derived from a conjugal mating.

[0030] Gene—a DNA sequence that encodes a polypeptide.

[0031] Genomic Library—a set of recombinant DNA cloning vectors into which segments of DNA, representing substantially all DNA sequences in a particular organism have been cloned.

[0032] Homology—degree of similarity between sequences

[0033] Hybridization—the process of annealing two single stranded DNA molecules to form a double stranded DNA molecule, which may or may not be completely base paired.

[0034] In vitro packaging—the in vitro encapsulation of DNA in coat protein to produce a virus-like particle that can introduce DNA into a host cell by infection kb—kilo base pairs.

[0035] KR—β-keto reductase.

[0036] KS—ketosynthase.

[0037] Mutagenesis—creation of changes in DNA sequence. They can be random or targeted, generated in vivo or in vitro. Mutations can be silent, or can result in changes in the amino acid sequence of the translation product which alter the properties of the protein and produce a mutant phenotype.

[0038] NmR—the neomycin resistance-conferring gene.

[0039] ORF—open reading frame.

[0040] ori—a plasmid origin of replication (oriR) or transfer (oriT).

[0041] PKS—polyketide synthase.

[0042] Promoter—a DNA sequence that directs the initiation of transcription.

[0043] Recombinant DNA cloning vector—any autonomously replicating or integrating agent, including, but not limited to, plasmids, comprising a DNA molecule to which one or more additional DNA molecules can be or have been added.

[0044] Recombinant DNA methodology—technologies used for the creation, characterization, and modification of DNA segments cloned in recombinant DNA vectors.

[0045] Restriction fragment—any linear DNA molecule generated by the action of one or more restriction enzymes.

[0046] Spinosyn—a fermentation product typically characterized by a 5,6,5-tricylic ring system, fused to a 12-membered macrocyclic lactone, a neutral sugar (rhamnose) and an amino sugar (forosamine), or a similar macrocyclic lactone fermentation product produced by a microorganism utilizing all or most of the spinosyn genes.

[0047] Spinosyn genes—the DNA sequences that encode the products required for spinosyn biosynthesis, more specifically the genes spnA, spnB, spnC, spnD, spnE, spnF, spnG, spnH, spnI, spnI, spnK, spnL, spnM, spnN, spnO, spnP, spnQ, spnR, spnS, S. spinosa gtt, S. spinosa gdh, S. spinosa epi, and S. spinosa kre, as described hereinafter, or functional equivalents thereof.

[0048] Subclone—a cloning vector with an insert DNA derived from another DNA of equal size or larger.

[0049] TE—thioesterase.

[0050] Transformation—the introduction of DNA (heterologous or homologous) into a recipient host cell that changes the genotype and results in a change in the recipient cell.

BRIEF DESCRIPTION OF THE FIGURES

[0051]FIG. 1 is a diagram illustrating the spinosyn biosynthetic pathway.

[0052]FIG. 2 is a map illustrating the arrangement of BamHI fragments and open reading frames in the cloned region of S. spinosa DNA.

[0053]FIG. 3 is a restriction site and functional map of Cosmid pOJ436.

[0054]FIG. 4 is a restriction site and functional map of Cosmid pOJ260.

[0055]FIG. 5 is a restriction site and functional map of pDAB1523.

BRIEF DESCRIPTIONS OF THE INVENTION

[0056] Spinosyn biosynthetic genes and related ORFs were cloned and the DNA sequence of each was determined. The cloned genes and ORFs are designated hereinafter as spnA, spnB, spnC, spnD, spnE, spnF, spnG, spnH, spnI, spnJ, spnK, spnL, spnM, spnN, spnO, spnP, spnQ, spnR, spnS, ORFL15, ORFL16, ORFR1, ORFR2, S. spinosa gtt, S. spinosa gdh, S. spinosa epi, and S. spinosa kre. The proposed functions of the cloned genes in spinosyn biosynthesis are identified FIG. 1 and in the discussion hereinafter.

[0057] In one of its aspects, the invention provides an isolated DNA molecule comprising a DNA sequence that encodes a spinosyn biosynthetic enzyme, wherein said enzyme is defined by an amino acid sequence selected from the group consisting of SEQ ID NOS 2-5,7-24, 26, 27, 29, and 33, or said enzyme is defined by one of said amino acid sequences in which one or more amino acid substitutions have been made that do not affect the functional properties of the encoded enzyme. In a preferred embodiment, the DNA sequence is selected from the group of genes consisting of spnA, spnB, spnC, spnD, spnE, spnF, spnG, spnH, spnI, spnJ, spnK, spnL, spnM, spnN, spnO, spnP, spnQ, spnR, spnS, ORFL15, ORFL16, ORFR1, ORFR2, S. spinosa gtt, S. spinosa gdh, S. spinosa epi, and S. spinosa kre, said genes being described by, respectively, bases 21111-28898, 28916-35374, 35419-44931, 44966-59752, 59803-76569, 20168-20995, 18541-19713, 17749-18501, 16556-17743, 14799-16418, 13592-14785, 12696-13547, 11530-12492, 10436-11434, 8967-10427, 7083-8450, 5363-6751, 4168-5325, 3416-4165, 2024-2791, 1135-1971, 76932-77528 and 77729-79984 of SEQ ID NO:1, bases 334-1119 of SEQ ID NO:27, bases 88-1077 of SEQ ID NO 24, bases 226-834 of SEQ ID NO 31, and bases 1165-1992 of SEQ ID NO:24.

[0058] In another of its aspects, the invention provides an isolated DNA molecule comprising a DNA sequence that encodes a spinosyn PKS domain selected from KSi, ATi, ACPi, KS1, AT1, KR1, and ACP1, said domains being described by, respectively, amino acids 6-423, 528-853, 895-977, 998-1413, 1525-1858, 2158-2337, and 2432-2513 of SEQ ID NO:2. In a preferred embodiment, the DNA sequence is selected from the group consisting of bases 21126-22379, 22692-23669, 23793-24041, 24102-25349, 25683-26684, 27582-28121, and 28404-28649 of SEQ ID NO:1.

[0059] In another of its aspects, the invention provides an isolated DNA molecule comprising a DNA sequence that encodes a spinosyn PKS domain selected from KS2, AT2, DH2, ER2, KR2, and ACP2, said domains being described by, respectively, amino acids 1-424, 536-866, 892-1077, 1338-1683, 1687-1866, and 1955-2034 of SEQ ID NO:3. In a preferred embodiment the DNA sequence is selected from the group consisting of bases 29024-30295, 30629-31621, 31697-32254, 33035-34072, 34082-34621, 34886-35125 of SEQ ID NO:1.

[0060] In another of its aspects, the invention provides an isolated DNA molecule comprising a DNA sequence that encodes a spinosyn PKS domain selected from KS3, AT3, KR3, ACP3, KS4, AT4, KR4, and ACP4, said domains being described by, respectively, amino acids 1-423, 531-280, 1159-1337, 1425-1506, 1529-1952, 2066-2396, 2700-2880, and 2972-3053 of SEQ ID NO:4. In a preferred embodiment the DNA sequence is selected from the group consisting of bases 35518-36786, 37108-38097, 38992-39528, 39790-40035, 40102-41373, 41713-42705, 43615-44157, and 44431-44676 of SEQ ID NO: 1.

[0061] In another of its aspects the invention provides an isolated DNA molecule comprising a DNA sequence that encodes a spinosyn PKS domain selected from KS5, AT5, DH5, KR5, ACP5, KS6, AT6, KR6, ACP6, KS7, AT7, KR7, and ACP7, said domains being described by, respectively, amino acids 1-424, 539-866, 893-1078, 1384-1565, 1645-1726, 1748-2172, 2283-2613, 2916-3095, 3188-3269, 3291-3713, 3825-4153, 4344-4638, and 4725-4806 of SEQ ID NO:5. In a preferred embodiment the DNA sequence is selected from the group consisting of bases 45077-46348, 46691-47674, 47753-48310, 49226-49771, 50009-50254, 50318-51592, 51923-52915, 53822-54361, 54638-54883, 54947-56215, 56549-57535, 58106-58990, and 59249-59494 of SEQ ID NO:1.

[0062] In another of its aspects, the invention provides an isolated DNA molecule comprising a DNA sequence that encodes a spinosyn PKS domain selected from KS8, AT8, DH8, KR8, ACP8, KS9, AT9, DH9, KR9, ACP9, KS10, AT10, DH10, KR10, ACP 10, and TE10, said domains being described by, respectively, amino acids 1-424, 530-848, 883-1070, 1369-1552, 1648-1726, 1749-2173, 2287-2614, 2640-2800, 3157-3341, 3422-3500, 3534-3948, 4060-4390, 4413-4597, 4900-5078, 5172-5253, and 5302-5555 of SEQ ID NO:6. In a preferred embodiment, the DNA sequence is selected from the group consisting of bases 59902-61173, 61489-62445, 62548-63111, 64006-64557, 64843-65079, 65146-66420, 66760-67743, 67819-68301, 69370-69924, 70165-70401, 70471-71745, 72079-73071, 73138-73692, 74599-75135, 75415-75660, and 75805-76566 of SEQ ID NO: 1.

[0063] In another of its aspects the invention provides an isolated DNA molecule comprising a DNA sequence that encodes a spinosyn PKS module, said module being selected from the group consisting of amino acids 6-1413 of SEQ ID NO:2, 1525-2513 of SEQ ID NO:2, 1-2034 of SEQ ID NO:3, 1-1506 of SEQ ID NO:4, 1529-3053 of SEQ ID NO:4, 1-1726 of SEQ ID NO:5, 1748-3269 of SEQ ID NO:5, 3291-4806 of SEQ ID NO:5, 1-1726 of SEQ ID NO:5, 1-1726 of SEQ ID NO:6, 1749-3500 of SEQ ID NO:6, and 35434-5555 of SEQ ID NO:6. In a preferred embodiment the DNA sequence is selected from the group consisting of bases 21126-24041, 24102-28649, 29024-35125, 35518-40035, 40102-44676, 45077-50254, 50318-54883, 54947-59494, 59902-65079, 65146-70401, and 70471-76566 of SEQ ID NO:1.

[0064] In another of its aspects, the invention provides a recombinant DNA vector which comprises a DNA sequence of the invention as described above.

[0065] In another of its aspects the invention provides a host cell transformed with a recombinant vector of the invention as described above.

[0066] In another of its aspects, the invention provides a method of increasing the spinosyn-producing ability of a spinosyn-producing microorganism comprising the steps of

[0067] 1) transforming with a recombinant DNA vector or portion thereof a microorganism that produces spinosyn or a spinosyn precursor by means of a biosynthetic pathway, said vector or portion thereof comprising a DNA sequence of the invention, as described above, that codes for the expression of an activity that is rate limiting in said pathway, and

[0068] 2) culturing said microorganism transformed with said vector under conditions suitable for cell growth and division, expression of said DNA sequence, and production of spinosyn.

[0069] In another of its aspects the invention provides a spinosyn-producing microorganism having operative spinosyn biosynthetic genes wherein at least one of the spinosyn biosynthetic genes spnA, spnB, spnC, spnD, spnE, spnF, spnG, spnH, spnI, spnJ, spnK, spnL, spnM, spnN, spnO, spnP, spnO, spnR, spnS, S. spinosa gtt, S. spinosa gdh, S. spinosa epi, or S. spinosa kre has been duplicated.

[0070] In another of its aspects the invention provides a spinosyn-producing microorganism, said microorganism having spinosyn biosynthetic genes in its genome, wherein at least one of said genes has been disrupted by recombination with an internal fragment of that gene, the rest of said genes being operational to produce a spinosyn other than the one that would be produced if the disrupted gene were operational. Preferably the microorganism is an S. spinosa mutant.

[0071] The invention also provides a spinosyn-producing microorganism having operational spinosyn biosynthetic genes in its genome, wherein said genes a) include at least one operational PKS module more than or at least one less than is present in SEQ ID NO:1; or b) include a PKS module that differs from the corresponding module described in SEQ ID NO:1 by the deletion, inactivation, or addition of a KR, DH or ER domain, or by the substitution of an AT domain. Preferably the microorganism is an S. spinosa mutant.

[0072] The invention also provides spinosyns produced by cultivation of the novel microorganisms of the invention.

[0073] In another of its aspects the invention provides a process for isolating spinosyn biosynthetic genes which comprises creating a genomic library of a spinosyn producing microorganism, and using a labeled fragment of SEQ ID NO:1 that is at least 20 bases long as a hybridization probe.

DETAILED DESCRIPTION OF THE INVENTION

[0074] A cosmid library of S. spinosa (NRRL 18395) DNA was constructed from fragments generated by partial digestion with Sau3A I. They were cloned into the BamHI site of vector pOJ436 (See FIG. 3) (Bierman et al., 1992) and introduced into E. coli cells by in vitro packaging and transduction. The library of recombinant bacteria thus prepared was screened for homology to two radiolabelled DNA probes by hybridization using the methods of Solenberg & Burgett (1989). One probe was the 400 kb SpeI fragment which is often deleted in non-producing S. spinosa strains generated by transformation or mutagenesis with N-methyl-N′-nitro-N-nitrosoguanidine (Matsushima et al., 1994). The second probe was a 300 bp piece of S. spinosa DNA that codes for part of a ketosynthase not involved in spinosyn biosynthesis (B. E. Schoner, personal communication). It includes a region which is highly conserved in all polyketide and fatty acid synthase genes, and was therefore expected to cross-hybridize with the spinosyn PKS genes. Cosmids 9A6 and 2C10 were two of seven clones that hybridized to both probes. Cosmid 3E11 was selected from the genomic library by hybridization to a radiolabelled SgrA1-BamH1 fragment of cosmid 9A6 (bases 26757-26936 in SEQ ID NO: 1). To determine the nucleotide sequence of the insert in cosmid 9A6, BamHI fragments were subcloned into the BamHI site of plasmid pOJ260 (See FIG. 4) (Bierman et al., 1992). The sequences of the inserts in these plasmids were determined by either of two methods. In one method, subcloned fragments were partially digested with Sau3A I, and size-selected pieces were cloned into the BamHI site of DNA from the phage M13 mp19. Single-stranded DNA was prepared from randomly selected recombinants, and sequenced by fluorescent cycle sequencing using reagents and equipment from ABI (Applied Biosystems, Inc., Foster, Calif.), according to the methods of Burgett & Rosteck (1994). The sequences from phage subclones of each plasmid were assembled into one contiguous sequence. In the other sequencing method, double-stranded plasmid DNAs were primed reiteratively with single-stranded oligonucleotides, each designed to complement a region near the end of previously determined sequence. The complete sequence was thus compiled from a series of partially-overlapping sequences. Prism-Ready Sequencing Kits (ABI) were used according to the manufacturer's instructions, and analyzed on an ABI373A Sequencer. The same strategy was employed to sequence across the BamHI sites of double-stranded 9A6 DNA. These data allowed the subcloned sequences to be aligned and oriented relative to one another using the AssemblyLIGN module of the MacVector program (Oxford Molecular, Campbell, Ky.), and thereby allowed the entire nucleotide sequence of the S. spinosa DNA in cosmid 9A6 to be assembled. The complete sequences of cosmids 2C10 and 3E11 were determined by the method of fluorescent cycle sequencing of random DNA fragments cloned in phage M13 (SeqWright, Houston, Tex.). The inserts in cosmids 2C10 and 3E11 overlapped, and the insert in 3E11 overlapped the end of the insert in cosmid 9A6. See FIG. 2. Together, the three cosmid inserts spanned about 80 kb of unique sequence (SEQ ID NO: 1). The following Table 3 identifies the portions of SEQ ID NO:1 included in each of the three inserts. TABLE 3 insert bases in SEQ ID NO:1 cosmid 9A6   1-26941 cosmid 3E11 23489-57287 cosmid 2C10 (corrected) 41429-80161

[0075]FIG. 2 gives a graphical representation of the relationship of the three inserts to the 80 kb of sequence.

[0076] It should be noted that cosmid 2C10 was missing bases G41877, C45570, C57845 and G73173 of SEQ ID NO:1. These deletions were determined to be cloning artifacts. The deletions generated in-frame stop codons that truncated PKS polypeptides. One of them occurred in a region also cloned in cosmid 3E11, but was not present in the region of 3E11 for which sequence was obtained. Uncloned DNA spanning all 8 stop codons in the PKS region was therefore sequenced directly from PCR-amplified regions of the genome of S. spinosa (NRRL 18395). The sequences from uncloned DNA confirmed the existence of the 4 stop codons at the end of ACP domains, and proved that the 4 frameshifts within other coding regions were cloning artifacts unique to cosmid 2C10.

PKS Genes

[0077] SEQ ID NO:1 includes a central region of about 55 kb with striking homology to the DNA encoding the polyketide synthases of known macrolide producers (Donadio et al., 1991; MacNeil et al., 1992; Schwecke et al., 1995; Dehoff et al., 1997). The spinosyn PKS DNA region consists of 5 ORFs with in-frame stop codons at the end of ACP domains, similar to the PKS ORFs in the other macrolide-producing bacteria. The five spinosyn PKS genes are arranged head-to-tail (see FIG. 2), without any intervening non-PKS functions such as the insertion element found between the erythromycin PKS genes AI and AII (Donadio et al., 1993). They are designated spnA, spnB, spnC, spnD, and spnE. The nucleotide sequence for each of the five spinosyn PKS genes, and the corresponding polypeptides, are identified in the following Table 4: TABLE 4 CORRESPONDING GENE BASES IN SEQ ID NO:1 POLYPEPTIDE spnA 21111-28898 SEQ ID NO:2 spnB 28916-35374 SEQ ID NO:3 spnC 35419-44931 SEQ ID NO:4 spnD 44966-59752 SEQ ID NO:5 spnE 59803-76569 SEQ ID NO:6

[0078] spnA encodes the initiator module (SEQ ID NO:1, bases 21126-24041) and extender module 1 (SEQ ID NO:1, bases 24102-28649). The nucleotide sequence and corresponding amino acid sequence for each of the functional domains within the initiator module and extender module 1 are identified in the following Table 5: TABLE 5 spnA AMINO DOMAIN BASES IN SEQ ID NO:1 ACIDS IN SEQ ID NO:2 KSi 21126-22379  6-423 ATi 22692-23669 528-853 ACPi 23793-24041 895-977 KS1 24102-25349  998-1413 AT1 25683-26684 1525-1858 KR1 27582-28121 2158-2337 ACP1 28404-28649 2432-2513

[0079] spnB encodes extender module 2 (SEQ ID NO:1, bases 29024-35125). The nucleotide sequence and corresponding amino acid sequence for each of the functional domains within extender module 2 are identified in the following Table 6: TABLE 6 spnB AMINO ACIDS DOMAIN BASES IN SEQ ID NO:1 IN SEQUENCE ID NO.3 KS2 29024-30295  1-424 AT2 30629-31621 536-866 DH2 31697-32254  892-1077 ER2 33035-34072 1338-1683 KR2 34082-34621 1687-1866 ACP2 34886-35125 1955-2034

[0080] spnC encodes extender module 3 (SEQ ID NO:1, bases 35518-40035) and extender module 4 (SEQ ID NO:1, bases 40102-44676). The nucleotide sequence and corresponding amino acid sequence for each of the functional domains within extender modules 3 and 4 are identified in the following Table 7: TABLE 7 spnC AMINO DOMAIN BASES IN SEQ ID NO:1 ACIDS IN SEQ ID NO:4 KS3 35518-36786  1-423 AT3 37108-38097 531-280 KR3 38992-39528 1159-1337 ACP3 39790-40035 1425-1506 KS4 40102-41373 1529-1952 AT4 41713-42705 2066-2396 KR4 43615-44157 2700-2880 ACP4 44431-44676 2972-3053

[0081] spnD encodes extender module 5 (SEQ ID NO:1, bases 45077-50254), extender module 6 (SEQ ID NO:1, bases 50318-54883), and extender module 7 (SEQ ID NO:1, bases 54947-59494). The nucleotide sequence and corresponding amino acid sequence for each of the functional domains within extender modules 5, 6, and 7 is identified in the following Table 8: TABLE 8 spnD AMINO DOMAIN BASES IN SEQ ID NO:1 ACIDS IN SEQ ID NO:5 KS5 45077-46348  1-424 AT5 46691-47674 539-866 DH5 47753-48310  893-1078 KR5 49226-49771 1384-1565 ACP5 50009-50254 1645-1726 KS6 50318-51592 1748-2172 AT6 51923-52915 2283-2613 KR6 53822-54361 2916-3095 ACP6 54638-54883 3188-3269 KS7 54947-56215 3291-3713 AT7 56549-57535 3825-4153 KR7 58106-58990 4344-4638 ACP7 59249-59494 4725-4806

[0082] spnE encodes extender module 8 (SEQ ID NO:1, bases 59902-65079), extender module 9 (SEQ ID NO:1, bases 65146-70401), and extender module 10 (SEQ ID NO:1, bases 70471-76566). The nucleotide sequence and corresponding amino acid sequence for each of the functional domains within extender modules 8, 9, and 10 is identified in the following Table 9: TABLE 9 spnE AMINO DOMAIN BASES IN SEQ ID NO:1 ACIDS IN SEQ ID NO:6 KS8 59902-61173  1-424 AT8 61489-62445 530-848 DH8 62548-63111  883-1070 KR8 64006-64557 1369-1552 ACP8 64843-65079 1648-1726 KS9 65146-66420 1749-2173 AT9 66760-67743 2287-2614 DH9 67819-68301 2640-2800 KR9 69370-69924 3157-3341 ACP9 70165-70401 3422-3500 KS10 70471-71745 3534-3948 AT10 72079-73071 4060-4390 DH10 73138-73692 4413-4597 KR10 74599-75135 4900-5078 ACP10 75415-75660 5172-5253 TE10 75805-76566 5302-5555

[0083] The boundaries and functions of the 50 domains identified in the foregoing Tables 5-9 are predicted based on similarities to the conserved amino acid sequences of the domains in other polyketide synthases, particularly the erythromycin polyketide synthase (Donadio et al., 1992). The unexpected KSi domain at the amino terminus of the initiator module is presumed to be non-functional because it contains a glutamine residue at amino acid 172, in place of the cysteine required for β-ketosynthase activity (Siggard-Andersen, 1993). A similar non-functional KS domain has been discovered in the initiator module of the tylosin PKS (Dehoff et al., 1997). The other spinosyn PKS domains are functional. None of them has the sequence characteristics of the inactive domains found in the erythromycin and rapamycin PKS genes (Donadio et al., 1991; Aparicio et al., 1996). The cloned PKS genes were shown to be essential for spinosyn biosynthesis by the discovery that strains of S. spinosa in which these genes had been disrupted were unable to produce spinosyns by fermentation. Gene disruption was achieved by cloning an internal fragment of the gene into plasmid pOJ260 (FIG. 4), using procedures well-known to those skilled in the art. The recombinant plasmids were then introduced into S. spinosa by conjugation from E. coli using the procedures of Matsushima et al. (1994), and selecting for apramycin-resistant exconjugants. Plasmids based on pOJ260 do not replicate independently in S. spinosa, and are stably maintained by integrating the plasmid into the chromosome via recombination between the cloned DNA and its homologous sequence in the genome. Integration creates two incomplete versions of the targeted gene (one lacking 5′ sequences and one lacking 3′ sequences) in the chromosome, with the pOJ260 DNA between them. Spinosyn biosynthesis was blocked by disrupting the spnA ORF with the BamH1 fragments V, N, or K, corresponding respectively to the following segments of SEQ ID NO: 1: 21365-22052, 22052-24338, or 24338-26227. Spinosyn biosynthesis was also blocked by disrupting the spnD ORF with BamH1 fragments G, E, or K, corresponding respectively to the following segments of SEQ ID NO: 1: bases 48848-50578, 50578-52467, or 55207-55888. Spinosyn biosynthesis was also blocked by disrupting the spnE ORF with BamH1 fragments J, I, D, H, and F, corresponding respectively to the following segments of SEQ ID NO:1: 63219-63989, 65406-66733, 66733-68997, 69369-70731, and 70731-72675. Spinosyn biosynthesis was not blocked by integration via BamH1 fragments C (bases 44612-47565 in SEQ ID NO: 1) or B (bases 55936-63219 in SEQ ID NO: 1) because they are not internal to any one gene; BamH1 fragment C spans the junction between spnC and spnD, and BamH1 fragment B spans the junction between spnD and spnE. In these cases, integration leaves one complete version of each gene.

Genes Adjacent to the PKS Responsible for Additional Modifications

[0084] In the DNA upstream of the PKS genes (cloned in cosmid 9A6) there were 16 open reading frames (ORFs), each consisting of at least 100 codons, beginning with ATG or GTG and ending with TAA, TAG or TGA, and having the codon bias expected of protein-coding regions in an organism whose DNA contains a high percentage of guanine and cytosine residues (Bibb et al, 1984). See the bottom right hand side of FIG. 2 for a graphical representation of the 16 ORFs in 9A6. Based on evidence that will be discussed hereinafter, 14 of the ORFs have been designated as spinosyn biosynthetic genes, namely: spnF, spnG, spnH, spnI, spnJ, spnK, spnL, spnM, spnN, spnO, spnP, spnQ, spnR, and spnS (they are labeled F through S in FIG. 2). In the following Table 10, the DNA sequence and the amino acid sequence for the corresponding polypeptide are identified for each of these genes, as well as for two ORFs (ORFL 15 and ORFL16) found immediately upstream of spnS. Also identified in Table 10 are the nucleotide sequences for ORFR1 and ORFR2 downstream of the PKS genes (in cosmid 2C10), and the amino acid sequences corresponding to them. TABLE 10 GENE BASES IN SEQUENCE ID NO: 1 POLYPEPTIDE spnF 20168-20995 SEQ ID NO: 7  spnG 18541-19713 (C) SEQ ID NO: 8  spnH 17749-18501 (C) SEQ ID NO: 9  spnI 16556-17743 SEQ ID NO: 10 spnJ 14799-16418 (C) SEQ ID NO: 11 spnK 13592-14785 (C) SEQ ID NO: 12 spnL 12696-13547 (C) SEQ ID NO: 13 spnM 11530-12492 (C) SEQ ID NO: 14 spnN 10436-11434 SEQ ID NO: 15 spnO 8967-10427 SEQ ID NO: 16 spnP 7083-8450  SEQ ID NO: 17 spnQ 5363-6751  (C) SEQ ID NO: 18 spnR 4168-5325  (C) SEQ ID NO: 19 spnS 3416-4165  (C) SEQ ID NO: 20 ORFL 15 2024-2791  SEQ ID NO: 21 ORFL 16 1135-1971  (C) SEQ ID NO: 22 ORFR 1 76932-77528 SEQ ID NO: 23 ORFR 2 77729-79984 SEQ ID NO: 24

[0085] To assign functions to the polypeptides identified in Table 10, three lines of evidence were utilized: similarity to sequences of known function, results of targeted gene disruption experiments, and results of bioconversion experiments.

[0086] The amino acid sequences of the predicted polypeptides were compared to sequences deposited in the databases at the National Center for Biotechnology Information (NCBI, Washington, D.C.), using the BLAST algorithm to determine how well they are related to known proteins. The BLAST searches of the NCBI databases were also repeated periodically to obtain new insights from additional homologies. Table 11 gives the best matches from a basic BLAST search on Jan. 12, 1998: TABLE 11 Significant GenBank BLAST Reported Gene Protein Match Accession Score* function spnF C-24 sterol methyl- U79669 202 C-methylation transferase (Zea mays) spnG Daunosamyl trans- L47164 202 sugar addition ferase dnrS (Streptomyces peucetius) spnH Mycinamicin III O- D16097 408 sugar methyltransferase methylation (Micromonospora griseorubida) spnI ORFY (Streptomyces Z48262 192 unknown nogalater) spnJ Hexose oxidase U89770 143 oxido- (Chondrus crispus) reduction spnK ORFY (Streptomyces Z48262 137 unknown nogalater) spnL C-24 sterol methyl- U79669 166 C-methylation transferase (Zea mays) spnM Unknown Z95586 132 unknown (Mycobacterium tuberculosis) spnN RdmF (Streptomyces U10405 409 unknown purpurascens) spnO 2,3 dehydratase Y11199 595 deoxysugar EryBV1 synthesis (Saccharopolyspora erythraea) spnP Mycarosyl transferase U77459 336 sugar addition EryBV (Saccharopolyspora erythraea) spnQ CDP-4-keto-6-deoxy- P26398 784 dideoxysugar D-glucose-3-dehydrase synthesis (Salmonella enterica) spnR Spore coat P39623 286 sugar polysaccharide transamination biosynthesis protein (Bacillus subtilis) spnS TDP-N- U77459 484 aminosugar dimethyldesosamine- methylation N-methyltransferase EryCVI (Saccharopolyspora erythraea) ORFL15 Keto acyl reductase Z11511 132 oxido- (Streptomyces reduction cinnamonensis) ORFL16 Regulatory protein of transcription the als operon, control (Bacillus subtilis) ORFR1 None ORFR2 Conjugation transfer Z99117 328 DNA protein replication (Bacillus subtilis)

[0087] In targeted gene disruptions, internal fragments were generated by PCR amplification from the cosmid DNAs, and cloned into plasmid pOJ260. The resulting plasmids were then conjugated into S. spinosa (NRRL 18395), and apramycin-resistant exconjugants were isolated and fermented. As stated earlier, the basis of disruption experiments is that when a plasmid bearing an internal gene fragment is integrated, two incomplete copies of the biosynthetic gene result, thereby eliminating the enzymatic function. Resulting fermentation products were analyzed to determine which spinosyns accumulated. The results of the targeted gene disruption experiments are summarized in Table 12.

[0088] In bioconversion studies, strains in which spinosyn synthesis was altered were tested for their ability to convert available spinosyn intermediates to other spinosyns.

[0089] The intermediates used were spinosyn A Aglycone (AGL), spinosyn P(P), spinosyn K (K), and spinosyn A 9-Psa (PSA). The results of the bioconversion experiments are also summarized in Table 12 TABLE 12 Internal Fragment in spinosyns Disrupted SEQ ID NO: accumu- Bioconversion products Gene 1 lated AGL→ P→ K→ PSA→ None None A + D spnF 20325-20924 None A A A spnG 18818-19426 None AGL K A spnG-H 18511-19559 P K A spnI 16699-17400 None J A A spnJ 14866-15470 None A A spnK 13785-14574 None spnL 12791-13428 None A A A spnM 11705-12371 3% A A A spnN 10636-11369 PSA spnO  9262-10226 PSA spnP 7391-8159 PSA PSA ORFL15 2145-2719 A + D ORFL16 1226-1852 A + D ORFR2 79321-79855 A + D

[0090] The conclusions drawn from BLAST searches, the gene disruption experiments, and the bioconversion studies will now be discussed in greater detail on a gene by gene basis.

[0091] The 11 genes upstream of the PKS were shown to be involved in spinosyn biosynthesis because strains in which they were disrupted failed to accumulate the major spinosyns A and D (Table 12). The next 2 genes upstream (ORFL15, ORFL16), and the large gene downstream (ORFR2) of the PKS, do not contribute to spinosyn production because fermentation was not affected by their disruption (Table 12). Disruption of the ORF immediately downstream of the PKS genes (ORFR1) was not attempted because it was too small to yield an internal fragment that would recombine at an acceptable frequency. Disruptions of the spnQ, spnR, and spnS genes were not attempted because early BLAST searches showed that these genes had striking similarity to enzymes known to be involved in the biosynthesis of unusual deoxysugars. spnQ had 53% identity between its gene product and the CDP-4-keto-6-deoxy-D-glucose-3-dehydrase involved in synthesis of the abequose moiety of the Salmonella enterica cell surface lipopolysaccharide (Jiang et al., 1991); spnR had up to 40% identity between its product and a group of proteins proposed to function as deoxysugar transaminases (Thorson et al., 1993); and spnS had 42% identity between its product and the SrmX product of Streptomyces ambofaciens, an organism that synthesizes the forosamine-containing antibiotic spiramycin (Geistlich et al., 1992). Even stronger similarities have emerged from recent BLAST searches (Table 11). Based on these similarities, and the close linkage of the genes to other spinosyn biosynthetic genes, it is concluded that spnQ spnR, and spnS are involved in production of the forosamine moiety of spinosyns.

[0092] spnF, spnJ, spnL, spnM

[0093] Strains disrupted in genes spnF, spnJ, spnL or spnM did not accumulate any spinosyns to significant levels (the low level of spinosyn A in the spnM mutant presumably resulted from some residual activity in the gene product deleted at its carboxy terminus). However, they bioconverted exogenously-supplied aglycone to spinosyn A, and therefore contained all the enzymes necessary for the later steps in spinosyn biosynthesis. These particular genes must be involved in generation of the aglycone from the putative monocyclic lactone product of the PKS genes. Roles for spnF and spnL in the formation of carbon-carbon bridges are consistent with their similarities to enzymes that methylate carbon atoms (Table 11). The absence of partially modified intermediates in the blocked mutants may result from instability of the compounds, or from reduced biosynthesis due to lack of glycosylated molecules to act as positive regulators, analogous to those of the tylosin pathway (Fish & Cundliffe, 1997).

[0094] spnG, spnH, spnI, spnK

[0095] Disruption of spnG also prevented spinosyn production, but the mutant strain could not bioconvert aglycone so this gene is required for a later step in the pathway (Table 12). Its sequence similarity to known glycosyl transferase genes (Table 11) suggests that spnG encodes the rhamnosyl transferase required for addition of the first sugar to the aglycone. The mutant with a disrupted spnG also lacked a functional 4′-O-methyltransferase (OMT) because it converted the 3′,4′-didesmethyl spinosyn (P) to the 4′-desmethyl spinosyn (K), but not to the fully methylated spinosyn A. The 4′-OMT activity was presumably not expressed in the mutant because the encoding gene (spnH) lies downstream of the disrupting integration in the same operon. The existence of this operon was confirmed by disrupting BamH1 fragment T, which spans the junction between spnG and spnH but is not internal to any open reading frame. Nevertheless, its disruption altered spinosyn synthesis, so this fragment must be internal to a single transcript that encompasses both genes. In addition to the expected loss of 4′-OMT activity encoded by spnH, this disruption also caused the unexpected loss of 3′-OMT function, leading to accumulation of spinosyn P (Table 12). The 3′ OMT activity appears to be encoded by the convergent downstream gene, spnI. This gene has most sequence similarity to the ORF Y gene of Streptomyces nogalator (Table 11). The function of the ORF Y product is unknown, but the organism produces an unusual tetra-methylated deoxysugar (nogalose) that is similar to the tri-methylated rhamnose of spinosyn A, so presumably both genes are involved in sugar methylation. Consistent with this hypothesis, disruption of spnI created a mutant that bioconverted spinosyn P only to the 3′-desmethyl spinosyn (J), not spinosyn A (Table 12). The disruption prevented any spinosyn accumulation in unsupplemented fermentations. spnK has a sequence similar to spnI and ORF Y, and presumably encodes the 2′-OMT. Its disruption also prevented accumulation of any spinosyns in unsupplemented fermentations (Table 12).

[0096] spnN, spnO, spnP

[0097] Disruption of genes spnN, spnO and spnP led to accumulation of the pseudoaglycone (Table 12). These genes are therefore involved in the biosynthesis or addition of the forosamine sugar. The similarity of spnP to glycosyl transferases (Table 11) indicates that it encodes the spinosyn forosamyl transferase. The high degree of similarity between spnO and a 2,3 dehydratase (Table 11) indicates that it is involved in the 2′-deoxygenation step of forosamine synthesis.

Rhamnose Genes

[0098] The overlapping inserts cloned in cosmids 9A6, 3E11 and 2C10 do not contain genes that encode the four enzymes required to produce rhamnose from glucose (Liu & Thorson, 1994). The first enzyme is a glucose thymidylate transferase (gtt), or equivalent enzyme, that activates glucose by addition of a nucleotidyl diphosphate (NDP). The second is a glucose dehydratase (gdh) to produce NDP-4-keto-6-deoxy-glucose, an intermediate common to many deoxysugar biosynthetic pathways. An epimerase (epi) and a ketoreductase (kre) specific for rhamnose synthesis are also required, to convert the NDP-4-keto-6-deoxy-glucose to NDP-L-rhamnose, the activated sugar that is the substrate of the glycosyltransferase adding rhamnose to the aglycone. Genes that code for these enzymes in S. spinosa were cloned from a separate library of 7-12 kb partial Sau3A fragments in the λ vector ZAP Express™ (Stratagene, LaJolla, Calif.). Radiolabelled probes were prepared by random primer extension (Boehringer Mannheim, Indianapolis, Ind.) of fragments from plasmid pESC1 containing the Saccharopolyspora erythraea gdh (Linton et al., 1995) and gtt genes. Plaque hybridizations to screen the phage library were performed with a stringent wash of 0.5×SSC, 0.1%SDS at 65° C. for 1 h. The plasmid (pDAB1620 and pDAB1621) portions of the vector containing inserts were excised from two of the three hybridizing phage, and partially sequenced using Prism-Ready Sequencing Kits (ABI) and multiple primers. The sequenced part of the insert in pDAB1620 (SEQ ID NO: 25) includes an ORF that would encode a 329-amino acid polypeptide (SEQ ID NO:26) with 82% identity to the gdh product of S. erythraea. Adjacent to this gene is an ORF coding for a 275-amino acid polypeptide (SEQ ID NO:27) with 72% identity to the S. erythraea kre gene product. The sequenced part of the insert in pDAB1621 (SEQ ID NO: 28) contains an ORF encoding a 261-amino acid polypeptide (SEQ ID NO: 29) with 83% identity to the S. erythraea gtt gene product. A second probe for rhamnose genes was prepared by PCR amplification of S. spinosa genomic DNA using degenerate oligonucleotide primers (SEQ ID NO: 30 and SEQ ID NO: 31) based on conserved amino acid regions in known epi proteins (Jiang et al., 1991; Linton et al., 1995). PCR reactions were performed in a GeneAmp 9600 Thermocycler with AmpliTaq polymerase (Perkin-Elmer) using 30 cycles of 30 sec at 94° C., 30 sec at 60° C. and 45 sec at 72° C. The probe hybridized to one phage in the 7-12 kb library; the plasmid portion of the vector containing this insert (pDAB1622) was excised and partially sequenced (SEQ ID NO:32). It includes an ORF for a 202-amino acid polypeptide (SEQ ID NO:33) with 57% homology to the S. erythraea epi protein. The genes were disrupted by recombination with plasmids containing internal fragments (bases 382-941 in SEQ ID NO: 25, 1268-1867 in SEQ ID NO:25, 447-994 in SEQ ID NO:28 or 346-739 in SEQ ID NO:32). Apramycin-resistant exconjugants were obtained in all cases, but they were only capable of growth on osmotically-stabilized media such as CSM supplemented with sucrose at 200 g/L, or R6 (Matsushima et al., 1994). Even under these conditions, they grew much slower than the parent S. spinosa (NRRL 18395), and were morphologically distinct, with highly fragmented mycelia. These results could be due to the presence of rhamnose in the cell wall in S. spinosa and a requirement that these four genes be present for normal cell wall synthesis in this organism. Mutants disrupted in these genes grew too slowly to be fermented under conditions known to produce spinosyns. However, Southern hybridizations of S. spinosa genomic DNA with the S. erythraea gtt/gdh probe (washed in 2×SSC, 0.1%SDS at 65° C. for 1 h) or with the degenerate epi probe (washed in 0.1×SSC, 0.1%SDS at 65° C. for 1 h) indicated that there are no other homologues of these genes present in the S. spinosa genome. Therefore, the four cloned S. spinosa genes must be the sole source of rhamnose for both cell wall formation and spinosyn biosynthesis.

[0099] The nucleotide sequence and corresponding amino acid sequence for each of the four S. spinosa genes required to produce rhamnose are identified in the following Table 13: TABLE 13 gene DNA sequence amino acid sequence S. spinosa gtt SEQ ID NO:28, bases 334-1119 SEQ ID NO:29 S. spinosa gdh SEQ ID NO:25, bases 88-1077 SEQ ID NO:26 S. spinosa epi SEQ ID NO:32, bases 226-834 SEQ ID NO:33 S. spinosa kre SEQ ID NO:25, bases 1165-1992 SEQ ID NO:27

[0100] Thus 23 genes from S. spinosa can be assigned roles in spinosyn biosynthesis: 5 PKS genes to produce a macrocyclic lactone, 4 genes to modify this to the aglycone, 5 genes to synthesize and add rhamnose, 3 genes to methylate the rhamnose, and 6 genes to synthesize and add forosamine. The hypothetical biosynthetic pathway is summarized in FIG. 1.

Utility

[0101] There are many uses for the cloned Saccharopolyspora spinosa DNA. The cloned genes can be used to improve yields of spinosyns and to produce new spinosyns. Improved yields can be obtained by integrating into the genome of a particular strain a duplicate copy of the gene for whatever enzyme is rate limiting in that strain. In the extreme case where the biosynthetic pathway is blocked in a particular mutant strain due to lack of a required enzyme, production of the desired spinosyns can be restored by integrating a copy of the required gene. Yield improvement obtained by integrating copies of spinosyn genes is illustrated hereinafter in Examples 1-3 and 6.

[0102] Novel spinosyns can be produced using fragments of the cloned DNA to disrupt steps in the biosynthesis of spinosyns. Such disruption may lead to the accumulation of precursors or “shunt” products (the naturally-processed derivatives of precursors). The fragments useful in carrying out disruptions are those internal to a gene with bases omitted from both the 5′ and 3′ ends of the gene. Homologous recombination events utilizing such fragments result in two partial copies of the gene: one that is missing the omitted bases from the 5′ end and one that is missing the omitted bases from the 3′ end. The number of bases omitted at each end of the fragment must be large enough so that neither of the partial copies of the gene retains activity. At least 50 bases will normally be omitted from each end, and more preferably at least 100 bases are omitted from each end. The length of the partial gene fragment should be large enough so that recombination frequency is high enough for a practical experiment. Useful fragments for disruptions are desirably at least 300 bases long, and more preferably at least about 600 bases long. Modified spinosyns produced by disrupting genes may be insect control agents themselves, or serve as substrates for further chemical modification, creating new semi-synthetic spinosyns with unique properties and spectra of activity. Example 4 hereinafter illustrates the use of disruption.

[0103] Novel spinosyns can also be produced by mutagenesis of the cloned genes, and substitution of the mutated genes for their unmutated counterparts in a spinosyn-producing organism. Mutagenesis may involve, for example: 1) deletion or inactivation of a KR, DH or ER domain so that one or more of these functions is blocked and the strain produces a spinosyn having a lactone nucleus with a double bond, a hydroxyl group, or a keto group that is not present in the nucleus of spinosyn A (see Donadio et al., 1993); 2) replacement of an AT domain so that a different carboxylic acid is incorporated in the lactone nucleus (see Ruan et al., 1997); 3) addition of a KR, DH, or ER domain to an existing PKS module so that the strain produces a spinosyn having a lactone nucleus with a saturated bond, hydroxyl group, or double bond that is not present in the nucleus of spinosyn A; or 4) addition or subtraction of a complete PKS module so that the cyclic lactone nucleus has a greater or lesser number of carbon atoms. Example 5 illustrates use of mutagenesis to produce a spinosyn with modified functionality.

[0104] The DNA from the spinosyn gene cluster region can be used as a hybridization probe to identify homologous sequences. Thus, the DNA cloned here could be used to locate additional plasmids from the Saccharopolyspora spinosa gene libraries which overlap the region described here but also contain previously uncloned DNA from adjacent regions in the genome of Saccharopolyspora spinosa. In addition, DNA from the region cloned here may be used to identify non-identical but similar sequences in other organisms. Hybridization probes are normally at least about 20 bases long and are labeled to permit detection.

[0105] The modified strains provided by the invention may be cultivated to provide spinosyns using conventional protocols such as those disclosed in U.S. Pat. No. 5,362,634.

[0106] The following examples are provided in order that the invention might be more completely understood. They should not be construed as limitations of the invention.

EXAMPLE 1

[0107] Improved Yield of Spinosvns A and D by Transformation With Cosmid 9A6

[0108] Vegetative cultures of S. spinosa strain NRRL18538 were grown in 50 ml CSM medium (trypticase soy broth 30 g/l, yeast extract 3 g/l, magnesium sulfate 2 g/l, glucose 5 g/l, maltose 4 g/l) in 250 ml Erlenmeyer flasks shaken at 300 rpm at 30° C. for 48 h. Fermentation cultures contained a 1 ml inoculum of this vegetative culture in 7 ml of INF202, a proprietary medium similar to that described in Strobel & Nakatsukasa (1993). The cultures were grown in 30 ml plastic bottles arranged in 10×10 modules, shaken at 300 rpm in a 30° C. room for 3, 5 or 7 days. Broths were extracted with 4 volumes of acetonitrile, then analyzed for spinosyns A+D by isocratic high pressure liquid chromatography (HPLC) through a C-18 reversed-phase column (Strobel and Nakatsukasa, 1993). The amount of spinosyns was determined from absorbance at 250 nm. For each time point, spinosyns A+D were determined from 10 fermentation bottles. Two representative samples from each set of replicates were also analyzed by a slightly modified HPLC system for pseudoaglycone (PSA), the spinosyn precursor which lacks forosamine. In this system the mobile phase is 35:35:30 acetonitrile/methanol/0.5% (w/v) aqueous ammonium acetate (R. Wijayaratne, unpublished).

[0109] The cultures contain not only the insect-active spinosyns A and D, but also pseudoaglycone (Table 14). TABLE 14 Spinosyn production in strain NRRL 18538 Time A + D (μg/ml) PSA (μg/ml) 3 d 101 ± 3  109 ± 11 5 d 269 ± 14 155 ± 26 7 d 334 ± 32 110 ± 53

[0110] The accumulation of the pseudoaglycone, a forosamine-deficient precursor of spinosyn A, suggests that, in this strain grown under these conditions, the yield of spinosyns A+D is limited by the supply and/or addition of forosamine

[0111] Cosmid 9A6 was conjugated from E. coli strain S17-1 (Simon et al., 1983) into S. spinosa strain NRRL 18538 using the method of Matsushima et al. (1994). Six independent isolates transformed with Cosmid 9A6 were subsequently grown and analyzed for spinosyn factor production under the fermentation conditions described above. The average yield of spinosyns A+D from these strains was higher than from their parent, by 35 μg/ml after 3 days of fermentation, and by 37 μg/ml after 5 days. The amount of pseudoaglycone in the transformed cultures was lower than in the parent strain throughout the fermentation (Table 15) TABLE 15 Spinosyn production in derivatives of NRRL 18538 transformed with Cosmid 9A6. Time A + D (μg/ml) PSA (μg/ml) 3 d 136 ± 4 31 ± 2  5 d 306 ± 5 7 ± 2 7 d 365 ± 7 7 ± 1

[0112] Strain NRRL 18538 and 6 independent isolates transformed with Cosmid 9A6 were analyzed for spinosyn content at different times during fermentation. For each strain, spinosyns A+D were determined from 10 fermentation bottles (Table 16). Two samples from each set of replicates were also analyzed for pseudoaglycone content (Table 17). TABLE 16 Effect of Cosmid 9A6 on spinosyn A + D in NRRL 18538 Time −9A6 +9A6 Effect of 9A6 3 d 101 ± 3  136 ± 4 +35% 5 d 269 ± 14 306 ± 5 +14% 7 d 334 ± 32 365 ± 7  +9% 9 d 414 ± 17 411 ± 8  −1%

[0113] TABLE 17 Effect of Cosmid 9A6 on pseudoaglycone accumulation in NRRL 18538 Time −9A6 +9A6 Effect of 9A6 3 d 109 ± 11 31 ± 2  −72% 5 d 155 ± 26 7 ± 2 −95% 7 d 110 ± 53 7 ± 1 −94% 9 d 119 ± 11 5 ± 1 −96%

[0114] It has therefore been demonstrated that transformation with Cosmid 9A6 can improve the efficiency with which precursor pseudoaglycone is processed to spinosyns. In NRRL 18538, the yield improvements for spinosyn A+D were 35% after 3 days of fermentation, and 14% after 5 days (Table 15). The rate-limiting process appears be the supply and/or addition of forosamine because pseudoaglycone was present in the parent at about 120 μg/ml throughout the fermentation, but in the transconjugants it was reduced to about 30 μg/ml at 3 days, and essentially depleted thereafter (Table 15). Although the conversion was not quantitative, the data are consistent with an improved efficiency in the processing of pseudoaglycone to spinosyn A+D in strains transformed with Cosmid 9A6. The effect could be the result of duplicating a forosamine biosynthetic gene, a forosaminyltransferase gene, or a combination of improvements. There was no statistically significant difference between the spinosyn A+D yields from the NRRL 18358 strains with or without Cosmid 9A6 after 7 or 9 days fermentation. Pseudoaglycone was still reduced in the transconjugants, but the extra spinosyn A+D produced by its conversion may not have been detectable against the higher background of spinosyns accumulated by this stage of the fermentation.

EXAMPLE 2

[0115] Correction of Methylation Deficiencies in Strain NRRL 18823 by Cosmid 9A6

[0116] Although spinosyn synthesis is limited by forosamine supply/addition in strain NRRL 18358, other biosynthetic functions may be limiting in other strains. S. spinosa strain NRRL18823 accumulates spinosyn H (2′-desmethyl-spinosyn A; Kirst et al., 1992), rather than spinosyn A. Spinosyn H is not an intermediate in the spinosyn A biosynthetic pathway, but a “shunt” product synthesized naturally when 2′-O-methylation does not occur. Cosmid 9A6 was conjugated from E. coli strain S17-1 into strain NRRL 18823 using the method described above. Two of the resulting exconjugants, when fermented, produced predominantly spinosyn A, with little spinosyn H (Table 18). TABLE 18 Strain H (μg/ml) A + D (μg/ml) NRRL 18823 323 0 NRRL 18823/9A6-2 36 551 NRRL 18823/9A6-5 45 646

[0117] This shows that transformation with Cosmid 9A6 is able to overcome a second type of limitation to spinosyn production—the methylation deficiency in strain NRRL 18823.

EXAMPLE 3

[0118] Correction of 4′-O-methylation Deficiency in Strain NRRL 18743 by Cosmid 9A6

[0119]S. spinosa strain NRRL18743 accumulates spinosyn K (4′-desmethyl-spinosyn A), an intermediate in the spinosyn A biosynthetic pathway. Two of the exconjugants of strain NRRL 18743 containing Cosmid 9A6 produced predominantly spinosyn A, with little spinosyn K, while the third produced no detectable spinosyn K (Table 19). TABLE 19 Strain K (μg/ml) A + D (μg/ml) NRRL 18743 488 0 NRRL 18743/9A6-1 38 829 NRRL 18743/9A6-2 22 725 NRRL 18743/9A6-3 0 706

[0120] This demonstrates that transformation with Cosmid 9A6 is able to overcome a third type of limitation to spinosyn A production—the methylation deficiency in strain NRRL 18743.

EXAMPLE 4 Accumulation of Spinosyn Precursor Caused by Disruption of spnP

[0121] An internal fragment of spnP (bases 7391-8159) was amplified in a polymerase chain reaction using primers given in SEQ ID NO:34 and SEQ ID NO:35. AmpliTaq polymerase (Perkin Elmer, Foster City, Calif.) was used according to the manufacturer's instructions, in a 100 μl reaction with 20 pmoles of each primer and 1 μg of 9A6 DNA. The mixture was subjected to 25 cycles of 60 sec at 94° C., 60 sec at 37° C. and 120 sec at 72° C. The amplification product was cloned as an EcoR1-HindIII fragment into the plasmid vector pOJ260 (Bierman et al., 1992), then conjugated from E. coli S17-1 into S. spinosa NRRL 18538. Stable exconjugants, resulting from a single homologous recombination event between the plasmid-born and chromosomal sequences, contain a copy of the vector DNA integrated into the chromosome between two incomplete copies of spnP. When fermented, these exconjugants accumulate the forosamine-deficient precursor pseudoaglycones, rather than the end products spinosyns A and D (Table 20). TABLE 20 Strain PSA (μg/ml) A + D (μg/ml) NRRL 18538 79 284 NRRL 18538/1614-2 416 22 NRRL 18538/1615-1 372 21 NRRL 18538/1615-2 543 21 NRRL 18538/1615-5 476 19 NRRL 18538/1615-6 504 18

[0122] The pseudoaglycones are intermediates useful in the preparation of known insecticides (International Application WO 93/09126)

EXAMPLE 5

[0123] Accumulation of a Novel Spinosyn Following Modification of the PKS Domain ER2

[0124] Overlapping, complementary oligonucleotides SEQ ID NO: 36 and SEQ ID NO: 37 were designed to modify the gene encoding the enoyl reductase function in module 2 of the spinosyn PKS. These mutagenic primers provide for substitution of the sequence TCACC in place of GGTGG at bases 33563-33567 of SEQ ID NO:1, so that the sequence encodes a serine-proline dipeptide instead of a glycine-glycine dipeptide in the putative NAD(P)H-binding motif A similar substitution was successfully used to inactivate an erythromycin ER without affecting any other PKS functions (Donadio et al., 1993). The substitution simultaneously introduced a novel PinA1 restriction site, and eliminated a SgrA1 site, to facilitate detection of the engineered DNA in recombinant organisms.

[0125] In the first step of the mutagenesis, two separate PCR amplifications were performed, one using the mutagenic primer SEQ ID NO: 36 and flanking primer SEQ ID NO: 38, the other using mutagenic primer SEQ ID NO: 37 and flanking primer SEQ ID NO: 39. In the second step, the products of the first reactions were diluted 100-fold, pooled and amplified with only the flanking primers SEQ ID NO: 38 and SEQ ID NO: 39. In the third step, the products of the second PCR reaction were cloned into the plasmid pCRII according to the manufacturer's instructions (InVitrogen, San Diego, Calif.). A portion of the mutated ER2 domain (spanning bases 33424-33626 in SEQ ID NO: 1) was excised as a Van911-NheI fragrment, and inserted in place of the wild-type Van911-NheI fragment in a 3.5 kb EcoRI fragment of cosmid 3E111 (bases 32162-35620 in SEQ ID NO: 1) cloned in the plasmid pBluescript SK-(Stratagene). The mutated EcoR1 fragment was then transferred into the conjugative plasmid pDAB1523 (FIG. 5), a derivative of pOJ260 containing the rpsL gene of Streptomryces roseosporus that confers a counter-selectable streptomycin-sensitive phenotype (Hosted & Baltz, 1997). The resultant plasmid containing the mutated EcoRI fragment was conjugated from E. coli S17-1 (Simon et al., 1983) into SS15, a spontaneous streptomycin-resistant derivative of S. spinosa strain NRRL18538, using the method of Matsushima et al. (1994). (Spontaneous streptomycin-resistant derivatives of S. spinosa strain NRRL18538 can be readily isolated by those skilled in the art.) Apramycin-resistant exconjugants were shown to contain both wild-type and mutated versions of the ER2 domain by Southern hybridization with digoxygenin-labeled probes (Boehringer Mannheim). They also contained the S. roseosporus rpsL gene and consequently, on BHI agar (Difco, Detroit, Mich.) containing streptomycin at 150 mg/L, they grew poorly and failed to produce aerial mycelium. Spontaneous revertants to streptomycin-resistance were selected on the basis of their ability to grow and produce white, aerial mycelium on BHI agar containing streptomycin at 150 mg/L. Southern analysis indicated that these strains no longer contained the S. roseosporus rpsL gene or any other pDAB1523 sequences. Some strains had lost the entire cluster of spinosyn biosynthetic genes, including the ER2 domain, as well as pDAB1523. In other strains the pDAB1523 sequences had been excised along with the mutant ER2 domain, re-creating the parental gene structure. In a third type of streptomycin-resistant strain, the pDAB1523 had been excised with the wild-type ER2 domain, leaving the mutated version in its place. When fermented, a strain of this third type produced a novel metabolite, separable from spinosyn A by liquid chromatography on a C18 column (ODS-AQ, YMC, Wilmington, N.C.) using a mobile phase of acetonitrile: methanol: 2% ammonium acetate (44:44:12). The new entity was analyzed by electrospray ionization and tandem mass spectroscopy (Balcer et al., 1996) using a triple quadrupole mass spectrometer (TSQ700, Finnigan MAT, San Jose, Calif.). It had the properties expected of the C18:C19-anhydrospinosyn A, with a mass of 729.5 daltons and produced the 142 dalton forosamine fragment. We conclude that modification of DNA encoding PKS domains results in the production of novel fermentation products.

EXAMPLE 6 Improved Yield of Spinosyns A and D by Transformation of NRRL 18538 With Rhamnose Biosynthetic Genes

[0126] Fragments containing the rhamnose biosynthetic genes were cloned independently into the conjugative vector pOJ260 (Bierman et al., 1992). The resulting plasmids are listed in Table 21. TABLE 21 Plasmid Genes pDAB1632 gtt pDAB1634 gdh + kre pDAB1633 epi

[0127] Each plasmid was conjugated from E. coli S17-1 (Simon et al., 1983) into S. spinosa NRRL 18538 by the method of Matsushima et al. (1994). Apramycin-resistant exconjugants, presumably containing a plasmid integrated into the chromosome by homologous recombination, were selected and fermented (Table 22). TABLE 22 Spinosyn production in derivatives of NRRL 15328 transformed with rhamnose genes Duplicated A + D (μg/ml) Strain Genes Experiment 1 Experiment 2 NRRL 18538 None 344 ± 39 405 ± 25 NRRL 18538/1632-1 gtt 410 ± 21 418 ± 38 NRRL 18538/1634-1 gdh + kre 351 ± 27 360 ± 21 NRRL 18538/1633-1 epi 318 ± 29 315 ± 18

[0128] In derivatives of NRRL 15328 transformed with gtt or epi, or the combination of gdh and kre, there was no consistent increase in the yield of spinosyns.

[0129] The fragments containing the gtt and gdh+kre genes were combined in a single plasmid. Two plasmids containing the combined gtt, gdh and kre genes (pDAB1654 and pDAB1655) were isolated, and conjugated from E. coli S17-1 (Simon et al., 1983) into S. spinosa NRRL 18538 by the method of Matsushima et al. (1994). Apramycin-resistant exconjugants were selected and fermented (Table 23). TABLE 23 Spinosyn production in derivatives of NRRL 15328 transformed with rhamnose genes Duplicated A + D (μg/ml) Strain Genes Experiment 1 Experiment 2 NRRL 18538 None 109 ± 9  133 ± 36 NRRL 18538/1654-2 gtt, gdh and kre 323 ± 19 244 ± 34 NRRL 18538/1654-5 gtt, gdh and kre 571 ± 23 412 ± 61 NRRL 18538/1654-6 gtt, gdh and kre 577 ± 17 425 ± 51 NRRL 18538/1654-11 gtt, gdh and kre 587 ± 23 426 ± 55 NRRL 18538/1655-1 gtt, gdh and kre 501 ± 20 395 ± 59 NRRL 18538/1655-3 gtt, gdh and kre 537 ± 27 421 ± 63 NRRL 18538/1655-5 gtt, gdh and kre 529 ± 21 428 ± 47 NRRL 18538/1655-12 gtt, gdh and kre 526 ± 26 401 ± 60

[0130] In derivatives of NRRL 15328 transformed with the gtt, gdh and kre genes, significant increases in spinosyn yields were observed. This probably results from overcoming a rate-limiting supply of NDP-4-keto-6-deoxy-glucose by simultaneously increasing the amounts of both gtt and gdh gene products, the enzymes necessary for its biosynthesis (see FIG. 1). A greater supply of the NDP-4-keto-6-deoxy-glucose intermediate would lead to increased production of both rhamnose and forosamine, and therefore greater ability to convert aglycone to spinosyns A+D. Consistent with the hypothesis that deoxysugar supply is limiting spinosyn production in NRRL 18538, many mutants blocked in forosamine synthesis or addition accumulate PSA to very high levels. More of this intermediate can be made because it requires only one deoxysugar, compared with the two required for spinosyns A or D.

[0131] The present invention is not limited to a particular vector comprising spinosyn genes of the invention, but rather encompasses the biosynthetic genes in whatever vector is used to introduce the genes into a recombinant host cell.

[0132] In addition, due to the degeneracy of the genetic code, those skilled in the art are familiar with synthetic methods of preparing DNA sequences which may code for the same or functionally the same activity as that of the natural gene sequence. Likewise, those skilled in the art are familiar with techniques for modifying or mutating the gene sequence to prepare new sequences which encode the same or substantially the same polypeptide activity as the natural sequences. Consequently, these synthetic mutant and modified forms of the genes and expression products of these genes are also meant to be encompassed by the present invention.

[0133] All patents and publications referred to above are incorporated by reference herein.

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1 39 1 80161 DNA Saccharopolyspora spinosa 1 gatctccatg aagctcaacg taggcacgga cggtcaggtg gactgggtga tcgcccgcga 60 cctgctggcc gacgggctga tcgccgaggc aggcgaaggc gatgtgcgga tcggccctcg 120 acggggtttt ccggggttgg tcgtgatcga gatgagctcg ccgtcggggc aggcctcctt 180 cgaggtgaat gctgaccagc ttgcggactt cttgaacgac acctacgacg tggtcgaacc 240 tggtgatgaa caccggtgga tgaacgtcga cgaggtgctg agccagctgc tctcgccaac 300 ctgtaatggc ccagctctcc cgaagcgccg cacgccaaag cgctggctgc gggacctggc 360 ggcgctgaac accgccacgc tgtgtctccg agctccagct ggaccacgtc ggtgccgtgc 420 gcccggctcg gtcaggccga aggtgctgat cttctccagg cgcgccatcg gcgcaggaag 480 cgctgcttct gctcccgccg cagtaccgtc gtgtcatggc cacggacagc ttcgattcct 540 cgaagctaca ggcggccgtg gcatcgagcg tcgcgtcgtg cgtctcggaa gtcagccgag 600 acgtctacac gcacctgatt accgaggctc cgcagttgcg agccgatgag atcgtcctca 660 gcattctacg gacgagtgtt gaggaaaata tcgccacatt gccgcacgtt ctcgaattcg 720 agattccgtt gggatattcg ccgggtcctg ctgcggtgtt ggagtatccg cgacgactgg 780 cgaaacattt ccatcaacgc gctgatcagg gccaaccgca tcgggcactt ccgcttcctg 840 tagtgatgcc tcgacgagat ccgccgccaa tgcgccgacg aggccgtatc cgcagcgacc 900 acgcaacgaa tgctcgcaac cagcttcggc tacatcgacc gcgtcacgga gcagatcgcc 960 gaaacctacc agctcgaacg ggaccgctgg ctcctggcga cgggacggcc gtgaggtctc 1020 tgcggcatcc gcatagcgtc ttctcccgct gaggcacatg aggtgttgcg cgcggtcgtt 1080 tccggcagtc gcacggcatt cgtcctagct gcgggcaatt gagggagcga agatttagag 1140 gagtgtggcc acgcggacca agccggcgag tgctcgggag cggctgtggg gcggccaggc 1200 gatgactgtc gtcacgtccg gcgcgtctag aaccggtacg gcggcgaggc cttcgagcag 1260 gttgacgcga ctggattcgg gcatgaccac ggtagtgcgg ccgagtgcga tcatttggaa 1320 cagttgcgtc tggttgcgta cttccacgcc ggggccatct ggatagacgc cgtcggggcc 1380 gggccagcgc gcaagcggga gatccggcag tgagctgaca tccgccatcc gtacatgggg 1440 ctcgctggca agcggatgcg aggtcggaag aatggcgact tgttgctcgg tgttcagaat 1500 ttcgatgtcg agttcggccg tcgggtcgaa gggttgatgc aacagcgcca cgtcggcccg 1560 gccgtcatgc agcgttttct ggggctggga ttcgcagagc agcaggtcga cggccacggc 1620 tcccggctcg gcggcgtacg cgtcgagcaa cttcgccagc agctcaccgg aggcgccggc 1680 cttggcagcc aggactagcg agggctggct cgtcgcggca cgctgggtgc gtcgctcggc 1740 tgctgccagc gcgccgagga tcgcccggcc ttcggtcagc agcattgccc cggcttcggt 1800 gagcgagact ttgcggctgg tgcgttgcag caacacgact ccgagtcgtt gctcgagctg 1860 ggcgatcgtc cgcgacagcg gcggctgggc gatgcccagg cgctgggcgg cccggccgaa 1920 gtgcaactcc tcggcgactg caacgaagta ccgcaactcc cgcgtctcca tccgtcgagc 1980 ctaccgctga ttcatatcag ctgggtatcg gtgtgagacc tagatggtgt tggttccccg 2040 ccggtttcgg gccacgctag aaagcatgag cgaacagacg attgcactgg tcaccggcgc 2100 aaacaaggga atcggatacg agatcgcggc cgggctcggc gcgctggggt ggagcgtcgg 2160 aatcggggca cgggaccacc agcgcgggga ggatgccgtg gcgaaattgc gtgcggacgg 2220 cgtcgatgcg ttcgcggtat ccctggacgt gacagacgac gcgagcgtcg cggctgctgc 2280 ggctctgctc gaggagcgcg ccggccggct cgatgtgctg gttaataacg ccggcatcgc 2340 cggggcatgg ccggaggagc cctcgaccgt cacaccggcg agcctccggg cggtggtgga 2400 gaccaacgtg atcggcgtcg ttcgggttac caacgctatg ctgccgttgc tacgccgctc 2460 cgagcgcccg cggatcgtca accagtccag ccacgtcgct tccctgacct tgcaaaccac 2520 gccgggcgtc gacctcggcg ggatcagcgg agcctactca ccgtcgaaga cgttcctcaa 2580 cgcgatcacc atccagtacg ccaaggaact cagcgatacc aacatcaaaa tcaacaacgc 2640 ctgccccggc tacgtcgcga ccgaccttaa cggcttccac ggaaccagca cgccggcaga 2700 cggtgccagg atcgccattc ggctcgccac gctgccagac gacggcccga ccggaggcat 2760 gttcgacgac gccgggaatg tgccctggtg aggcgctcag tcggcgatgg tgcaatcgaa 2820 gtcggagagg ctcgctgcga ccgggtacgc cgaacaacac ctgttcctgt gggtacggat 2880 gtcggccttc gccgtctcgg tcattgacaa cctgtacttc gggcgccgtt accgccggtg 2940 cgccgcggtt gcctggcgac actgggccag ccgtggctca ccggcggctt aggtcaggcg 3000 tgggcggttg ccagcatggc gggtgcggct ttgcgtaggt cgggtaggcg catccggcgc 3060 gggagccggt cgagttcttc gccgatggcc ggtgctttgg ggctgctcag gagccgaaca 3120 cctcccagcc gcaggtgccg ggctgaaccg agtggttctc gtcggctcgg atcacaacgt 3180 ctgccggaac agctgcggcg aggtggtcgc agattcgagg cgggatcgtc ctcggcgacc 3240 ttgccgacga tcgcggctag ggcccagggc ttcgtcgacc tggttggcac ctagatcacg 3300 acggtcaaaa cttgccggca tcagagacga tcgaagtgat cccgggtcac gtcggcttat 3360 cggtcgagtg agtcccgggg cctgcccagc caggtcttgc gtcgttgttc cgggctcagt 3420 tgcggattcc gacgaacagg cctcggccgt tcggtgctcc aggaaggtat tccgcgcgga 3480 tccctgcgtc ttcgagcgcg gcggtgtact cgtcctcagt gaacagcgag aggatttcga 3540 actctgtgaa gtcccggatc ccggtgggtt cggcgactgt gtagcggacg gtcatccggc 3600 tcgtacggcc ctccaggacc gagtgcgata gccggctgat cacccgctcg ccgtggtgcg 3660 cgacggctcc ggtgacgaac ccgtcgatga acttgtcggg aaaccaccag ggttcgatga 3720 ccgcgactcc accaggggcc aggtgccggg ccatgttccg cgtcacgcgt cgcaggtcgt 3780 caacggtccg catgtaagcc gcggtaaagc acaggcaggt gatgacgtcg aatggctcgc 3840 cgaggtcgaa atcgcggatg tcaccgatgt gaatcggtac ctcagggact cgtctgatcg 3900 cgatctcccg catcgcatcg gacagttcaa gccccgcgac cttcgcgtat tcggcacgga 3960 atcgctctag gtgcgccccg gtcccacagg cgacgtcgag tagggactgt gcttcgggca 4020 gcctggtgcg tacgagctgg actacttccc cggcctcggc tgcccagtcc cggccacgcg 4080 cggagtggat cgcgtcgtag atgtcggcat gatctgggct gtataccgag gaggtttctg 4140 cgaatgtgtc gctcacgcgc gacatcctca ctttcggagt ggtgatcttt ggctgatgtg 4200 gtgttcgacg gccttctgga actcgtcagc caccgtgcgc acctcggcgt cgtcaaggct 4260 tgggtgcagt ggtagcagga gtgttctgcg gcaggcgtcc tccgcagaag gcagcttgca 4320 gtccgcgcgg tagatgggga ccttgtgcag gggcgggtag cggtagctcg tgtagatgcc 4380 gcgttccagc atttgctgcg ccacctggtc gcggatctcc ggagccagct ggacccagta 4440 gaagtagtgt gacgagacgt gcccatccgg tagcgtcggc ggtaggagga cacccggcac 4500 atcggaaagc aaccggtcgt actgcgtagc gatttctcta cgcctgttga tgaattctgg 4560 cagtttgcgc agctgcacgc tgccaagcgc tgccgtcatg tcgttcccga tcagccgctg 4620 gccgatgtct tcgacgcgaa tatcccacca gcggttggaa gacttggccg aatcgaatcc 4680 gctcatctgc tcaagaccgt ggtaggcgag tcgtcttgcg cggtgcgcca gctccggatc 4740 cgccgcgtag aacatgcccc catccccggt gaccaggatc ttcatcgcat cgaaactcca 4800 cgtggccagg tcaccaaagg ttccgcaagc ggtgccgtgc acggacgatg ccaccgcgca 4860 ggcggagtcc tcgatgagca tgaggccctt ttcacggcag aaatcggcga tcgcggtgac 4920 ttctcccggc gatcctccat agtggagcag caatacggcc ttggtcgccg gcgtgatggc 4980 cctcgccaca tcatccagcg tggggttcaa cgtccggggg tcgacgtcgc agaacaccgg 5040 gcgggcaccg gaggatgcga tggcgttggc cgccgccacg aagcttatcg aaggaagtac 5100 cacgtcgtcg cctgggccga ggtcgagcac ctgcacggta aggaacagcg cggcagtccc 5160 cgagttgagg aacacgacct gttcgggatc cactcccagg tggtgggcga attcggcctc 5220 gaacgtccgg gtgcgcggcc cgagcccgat ccagttggag gcgaacacct ccgcgatcgc 5280 gtcgagttct tcggtgccga ggatcggctg gtgcaggttg atcacgttgc tgaaatcctc 5340 cgagatgccg ccatgctgga tgctaggaac tcttggccac gaattcagcg attgattcga 5400 cgacgtagtc gatcatttgg tccgttatgc ctgggtagac gccgacccag aaggttcggt 5460 cggtgacgat gtcgctgttg gtgagcgcgt cggcgatccg gtaccgcacc tgctcgaagg 5520 ccgggtgccg ggtgatgtta ccgccgaaca gcagtcgggt gccgatgttg cgggattcca 5580 ggaagttcac cagggcggca cgggtgaacc cggcgtccgc actgatggtg atcgcaaacc 5640 cgaaccagct cgggtcgctg tgcggtgtgg ctaccggcag cagcaggccc ggcaacccgg 5700 acagcccttc gcgcaaccgt cgccagttac ggcggcgtgc cgacccgaat gcggaaatct 5760 tgctcaactg gctcagcgca agtgcggcct gcaggtcggt ggtcttgagg ttgtaaccga 5820 cgtgggagaa cgtgtacttg tggtcgtagc ccggtggaag ggtaccgagg tggtagtcga 5880 acctcttgcg gcaggtgttg tccacgccgg gctcgcacca gcaatcccgt ccccagtcac 5940 gcagcgactc gatgatgcga gccaattcca ggctgccggt caacacgcag ccaccctcgc 6000 cgctggtgat gtgatgggca ggatagaagc tgaccgttgt caggtcgccg aaggttccgg 6060 tcagccgtcc ccggtaggtg gatcccaccg catcacagtt gtcttcgacg aggaacagct 6120 cgtgttcttt tgcgatctcc gcgatttcgt cagcggcgaa ggggttgccc agggtgtgcg 6180 ccagcatgat ggctcgcgtc cgttccgtga cggcggcctt gatgcggtct ggcgttgcgt 6240 tgtaggtgcc cagttccacg tcgacgaata ccgggacgag tccgttttgg accgccggat 6300 tgatcgtcgt ggggaagccg accgccgcag tgatcacttc gtcgccgggc cgcagtcgtg 6360 cctcgccgag tttgggggag gtaagcgaac tcagtgccag gagattggcc gacgaaccgg 6420 agttgacgag atgagccttg cggaggccga agaagcgggc gaactcgctc tcgaatcgcc 6480 gtgcattccc gcccgcggcg atccggagct ccagcgcggc ttccaccagt gccacccggt 6540 cgtcctcgtc gagcacggcg cccgatggcc ggatcggcgt cgatccagcc acgaaggtcg 6600 gggattcctg ttcgcggtgg taatcgcgta cggatgccaa tatccggtcc ttggcatccg 6660 gcaccatctc agtagcggta gcgcaagtgt cgtcacacga agtcactctg gcgcgccctt 6720 tccccagcgc tctggttttc cggctctgca tgcaggcgac gatcagtctt cgcgccttgc 6780 cttcaggaga tgagcgatgc ccgtggcgaa tcgcgttatg acgtcccagc gggacagtgt 6840 gctgtctcgg cgccttacac cttcctgccc tggttcgatg cggtgcggga catcaggaca 6900 gcggagcaag gagaagcgct cattgactca gaaatcctcg atctacccgg cacacccgac 6960 tcggtagagc ccaggctagc gggaacgacc tgctcgcgct tgtcaagatc gctaccatca 7020 cctggaaggc ctaagatttg gcttgcgaaa gcggcgtttc ccgggggata tcagagattt 7080 ctgtgattct tggcatgctt cccgggtgtt caattgcgat cggagagttc atgcgtgtcc 7140 tgttcacccc gctgccggcg agttcgcact tcttcaacct ggtgccgttg gcgtgggcgt 7200 tgcgtgccgc ggggcacgag gtccgtgtcg ccatctgccc gaatatggtg tcgatggtca 7260 ccggagcagg actcaccgcg gttcccgtcg gcgacgagct cgacctcatc tccttggcgg 7320 ccaagaacga actcgttctc ggcagcgggg tctcgttcga cgagaagggg cggcatccgg 7380 aactcttcga cgagctgctg tcaatcaact ccggcagaga cacggacgcc gtggagcaac 7440 tccaccttgt ggatgaccga tcgctggacg atctcatggg gttcgccgag aaatggcagc 7500 ctgatctcgt tgtgtgggac gctatggtgt gttcggggcc agttgtggcg cgagcgctcg 7560 gcgcacgaca cgtgcggatg ctcgtcgccc tcgatgtgtc ggggtggctg cggtccggtt 7620 tcctcgaata ccaggaatcg aagccgcctg agcagcgcgt cgacccgctc gggacgtggc 7680 tgggagcgaa gctcgccaag ttcggagcca cgttcgatga agagatcgtg acgggccaag 7740 cgaccataga tccgattcca tcctggatgc gcctgcctgt ggacttggac tacatctcga 7800 tgcgtttcgt gccgtacaac ggtccggcgg tgttgccgga gtggttgcgc gaacgaccga 7860 cgaagccgcg cgtctgcatc acgcgcgggc tgaccaagcg gcggctgagc agggtgaccg 7920 aacagtacgg ggagcaaagt gaccaggaac aagcaatggt ggaaaggttg ttgcgcggcg 7980 cggccaggct cgacgtcgag gtgatcgcca ccttgtctga cgacgaagta cgggagatgg 8040 gggagttgcc ctcgaacgtc cgggtccacg aatacgtacc gctcaacgaa ctgctggagt 8100 cgtgttcagt gatcatccat catggctcga cgacgacgca ggaaaccgcc acggtcaacg 8160 gcgtaccgca gttgattctc cctgggacct tctgggacga atctcgtagg gcggagctcc 8220 tagccgatcg gggagccggt ctggtcctcg accccgcgac gtttaccgaa gacgacgtgc 8280 gaggtcagct ggcccgcctg ctcgacgagc cgtcgttcgc tgccaacgcg gcgctgatcc 8340 gccgtgaaat cgaggaaagt cccagcccgc acgacatcgt tccacgtctg gaaaagctag 8400 ttgccgaacg tgagaaccgc cgcactgggc agtctgatgg ccatccgtga gcaacgtgtg 8460 gccggaaaca tggacgccgg ggtttggcag gtgttcatcg ctgttgcgtc gactcggatt 8520 ccgccgtgac cgggacgatg ccaggcgagt cccgaagtca gattcttgtc cagaatcgtc 8580 caatggggtg ttgatctccc cagaggtttg cgctccaacc gatttccgac gaggatcgtg 8640 gcgcccgctg agcaacgact accgtgcggt cgagacatac cgctgtgcgc caggagcgaa 8700 ggtgggttgc ccgatcaccg tgctggtggt agatgccgag ccgaaggtca ccttggatga 8760 ggcggaagcc tggcgagagc acaccgaggc cgtggccgac gtccgtgtct tctccggcgg 8820 gcatttcttc atgaccgaac gccaggacga ggtgctcgcg gtccttacgg gcggatcgct 8880 tcgatgatcc tcgccaggcc gctggaccag accgcgacgc ccctgggagc cggcgtgcac 8940 atcgtcacgg cagtgaggga ttgggcatga gcagttctgt cgaagctgag gcaagtgctg 9000 ctgcgccgct cggcagcaac aacacgcggc ggttcgtcga ctctgcgctg agcgcttgca 9060 atggcatgat tccgaccacg gagttccact gctggctcgc cgatcggctg ggcgagaaca 9120 gcttcgagac caatcgcatc ccgttcgacc gcctgtcgaa atggaaattc gatgccagca 9180 cggagaacct ggttcatgcc gacggtaggt tcttcacggt agaaggcctg caggtcgaga 9240 ccaactatgg cgcggcaccc agctggcacc agccgatcat caaccaggct gaagtaggta 9300 tcctcggcat tctcgtcaag gagatcgacg gcgtgctgca ctgcctcatg tcagcaaaga 9360 tggaaccggg caacgtcaac gtcctgcagc tctcgccgac ggttcaggca actcggagca 9420 actacacgca ggcacaccgt ggcagcgttc cgccctatgt ggactacttc ctcgggcggg 9480 gccgcggccg cgtgctggta gacgtgctcc agtctgaaca ggggtcctgg ttctaccgga 9540 agcgcaaccg gaacatggtg gtggaagtcc aggaggaagt gccagtcctg ccagacttct 9600 gctggttgac gctcggccag gtgctggctc tccttcgtca ggacaacatc gtcaacatgg 9660 acacccggac ggtgctgtct tgcatcccgt tccacgattc cgccaccgga cccgaactag 9720 ccgcctcgga ggagcccttc cgacaggcgg tggccaggtc gctctcgcac ggcatcgatt 9780 cgtcgagtat ctccgaggcg gtcggttggt tcgaggaagc caaggcccgc taccgcttgc 9840 gggcaacgcg cgttccgctg agcagggtcg acaagtggta tcgcaccgat accgagatcg 9900 cccaccagga cggcaagtac ttcgcggtga tcgcggtgtc ggtgtccgcg accaatcgtg 9960 aggtcgccag ctggacgcag ccgatgatcg aaccgcgaga acaaggtgag atcgcactgt 10020 tggtcaagcg gatcggcgga gtgctgcacg gtttggtcca cgctcgggtg gaggctgggt 10080 ataagtggac tgcggaaatc gctcccacgg tccagtgcag tgtggccaac taccaaagca 10140 ccccgtcgaa cgactggccg ccgttcttgg acgacgtgct caccgccgat cccgaaaccg 10200 tgcggtacga atcgatcctg tccgaagaag gcggtcggtt ctaccaggcg cagaacaggt 10260 accggatcat cgaggtgcat gaggacttcg cggcacgacc tcccagcgac ttccggtgga 10320 tgactttggg acagttgggc gagctgctcc ggagcaccca cttcttgaac atccaggcgc 10380 gcagcttggt cgcctccctg catagcttgt gggcgttggg gcgatgacca gctcgatgcg 10440 aaagccggtg cgcatcggtg tgctcgggtg cgcttccttc gcgtggcgac ggatgctgcc 10500 cgcgatgtgc gacgtggccg aaacagaggt ggtggcggtg gcgagccgtg atccggcgaa 10560 agccgaacgg ttcgcagcgc gattcgaatg cgaggcggtg ctgggttacc agcggctcct 10620 ggagcggccg gacatcgatg ccgtctacgt gccgttgccg cctggcatgc atgcagagtg 10680 gatcggcaag gcgcttgagg cagacaaaca cgtgcttgcg gagaaaccgc tgacgacgac 10740 ggcgtccgac accgctcgcc tggtcgggct ggccaggagg aagaacctgc tgctgcggga 10800 gaattacctg ttcctccacc acggccggca cgacgtggtc cgcgacctgc tgcaatccgg 10860 ggagatcggt gagctccggg agttcaccgc cgtgttcgga attccgccgc ttcccgacac 10920 ggacatccgc tatcgcaccg aactcggtgg cggagcgttg ctggacatcg gtgtctatcc 10980 cgcccgtgcc gctcggcact ttctcctcgg tccgctcacg gttctcggcg caagctcgca 11040 cgaggcccag gagtcgggcg tcgacttgtc gggcagcgtg ctgctccaat cggaaggtgg 11100 caccgttgcc cacctcggat acggtttcgt gcaccactac cgcagcgcgt acgagctgtg 11160 ggggagtcgt gggcgaatcg tcgtcgaccg ggcgttcacg ccgcccgccg agtggcaggc 11220 cgtgatccga atcgagcgga agggcgttgt cgacgagttg tccttgccag cggaagatca 11280 ggttcgcaag gcggtcaccg ccttcgcacg cgacatcaga gcagggacag gcgtggacga 11340 ccctgcggtg gccggagatt cgggcgaatc gatgatccag caggccgcgc tggtggaggc 11400 gatcggtcag gcccgtcggt gcgggtccac atagccgccc ggcatccgcg ggtagtagtt 11460 cgcctcgaag cctgaccggg catccggaag ccagcgggga agccgctgga gaggctcacc 11520 gccatccgct cacctggcat ctcgcggacc gctgatcgcg gacggctcgg agaagtgctc 11580 gtcgaaccac gagacgacca ctcgcgagct ggccagggcg gcgggaaagt gagccaatcc 11640 ggagagcgga tgccaccgca ctggcgtacc cgccgcgcgg tagctgtccc ggagtcgctc 11700 gccgaatgcg aacggaacga tctcgtcgtc cgtgctgtgg tagacgagcg tggggaccac 11760 cgggccaccg ttcctacctg cgacgctttc ggccagtcgt gcgcgccatc gaggttgctc 11820 gaaaaggccg gaagtgtcga ggaagtcgct cagctcgcgg ccgaggaagc gggtgacgag 11880 ctccggtgca ccgagctcgc gcacttgatc aacggcggta cgacccgctt cggtgagaag 11940 ctcgtcgaat ggcagatcgg ggtaggcagc ggcatgcccg accaggccgg ccagcaccgg 12000 cccggtgaac accccgtcat ttcggtggat gatgtccagc agatcgatcg gcaccgcacc 12060 tgcggccgca gcgcggattc gcagttcagg tgcgtaggtg gggtgcagtt cgccggcgaa 12120 ggccgacgct tgcccaccct gcgcatagcc ccagatgccg accgggcagt cggtcgtcag 12180 gccggagccc ggtagccgtt gcgcagcgcg ggcggcatcg agcatggcgt gtccctgcgc 12240 cctgccgacg gtgtaggtgt gggttccagg agtaccgagg ccttcgtagt cggtgatgac 12300 cacggcccac ccgcggtcga gggccacggc gatcagctcg gtctccggct cggttccggt 12360 tcgaagcagg tacgacgggg caacttggct accgaggccg tgggtgccca ctgcgaaagt 12420 gatgatgggg cgatcttcgc gcggccacgg gatgttcggc accagaacgg tgccggagac 12480 ggcgttcggc atgccaaggg cggagttgga ccggtagagg atttgccagg ccttggctgc 12540 gacgggttcg cccgtgccgc gcagtgccga gacgggccgg gccctgagga gcgtgcccgg 12600 gacacccggc ggtagcggcg tcggcggtcg gtagaaggga tcatccgcgg gtgcccgcag 12660 atcgtcgccg accaggctgg cgtgctcgga ggccatcagg actgcttctt tcgagcctgc 12720 aggagcatga aacccatgct ttcctcgttt ctggcgtaat ccggatgttt ccggtattcc 12780 gcaaccgcgg cgatcagctg tgctggtccc ggtccgtgct tcgccgcgat gtctcccaag 12840 tagcgttgct ggtaggtgcc gacagccgca ggctcgacgc cggcgagctc atcgagtttc 12900 cggagcaact cgtcgacgta ccaggagacc atgcacctgg tctgtgccgt gaggtcggtg 12960 acttcgagaa tctcgaaccc ggcttcgctg accagcgccg tgaagctgtt caaggtatgg 13020 gcggtcgtgc ccgtccaaac cgccgcgtac tcttccggga gtcgaacccg agtgatgatg 13080 tctccgagga cgaaccggcc gccgggttcc aggattcggt ggacctcgcg gatcgcggcg 13140 gcctggtcca cgatctgcac gacggactgc atcgcccatg cggcctgaaa gaaaccgtcc 13200 gggtagggca gctgggcgcc gtcgactaga tcgaactcaa gactgccggc cagtccggtc 13260 tcgttggcga gcctggtggc ggcggcgaga tgctgggcgt tcacggtgat tccggtgact 13320 cgaacgccgc tggcgcatgc cgcacggact acgggctgcc cattgccgca gcccaggtcg 13380 aacaggtgcg ctccgggacg gagcgcggcc ttgtcgatga acaggtcggt cagttggtcg 13440 gcagcatccg accacggtgt ggcaccggca tcctcccgat acccgcccgc ccagtaaccg 13500 tggtgcaggg gacgcccgtg cgccaacgca tcgaagatgg actccacctg atccgcggtc 13560 ggaaatgcct gtgtgttcgc ccctctgctg ttcactcgtc ctccgcgctg ttcacgtcgg 13620 ccaggtgcaa tatgtcgtcc agactccttg gcacccaagc aggaacgccg ccttcggcgt 13680 tgacgccttt ctccaggaac gcgatgttgt ggtaggtgtg gaggccgacc aaattgcgtt 13740 ccaggtagct cggctcgtac gagcccgcat gcggctgctc ctcgtgctga acgccttcca 13800 acaggttctt gagcaggctg accgtggtgc cgggtgcggc cgggcactgc gcctgcccgc 13860 cgaatccggg agcataggtc gtccacagat cctcgatcac gtatacgcca ccgctgcgca 13920 accgggggaa cagcgtttcc agggatgtgc gcacgtgtcc gttgatgtgg ctgccatcgt 13980 cgatgatgat gtcgaacggt ccgtacttgt cgtcaacggc ggccagctcc tcgggcttgc 14040 tctggtcggc gcggacggtg cagagcctct gctggtcgag gaaggacttg tcgaaaacgt 14100 ccatcccgaa cacgaggccg cggtggaagt agcgcttcca catcttcagg gattcgccgc 14160 cgccaccgtc gaagttgtag ccaccgacac cgatctccag gatgcgcacc gggcgatcac 14220 ggaactcgcc gaggtgtcgc tcgtatagcg gggtgaacca gtgcaggccg ccccacttgt 14280 ccgtgcggta gtgggaggcg agcaagttga ggtcgggacg tcggtgcccg cagccggcga 14340 ccactgcgga gatggcctgg aagccatcgg acagttccga cggaccgggt atcgaaccgg 14400 atgtggtggt tcggaggaag ttggtgctcc gggcgccgac ggccctggga gctcctgggc 14460 cgaacaactc ggcgatgaga tcggtgagct cgtaaccgat ccgcagcggg acgtctccga 14520 ccggtcgttg ctcggccttg atcagctcac cggactgtag cgtcaggacg aagtcaacgg 14580 tctcgcctcg gtgggtgatc tggaccgcga cctcggtccg ttcgatgtcg ggggccggtt 14640 ccgcgcggaa gaggatctcg tcgatcagca cgggtgcgat cctggcgagt ccgagttcgg 14700 tggtcaggtc ggccaggctc gccgcactgg atccggcggc gaggatgatg cgttccacgg 14760 tttcgatctc gtgcgttgtg gacatcgtga tgagctcctc atggctgacc gggtgaaagc 14820 cgtgccggcg gtttgatcga caggccgtgc tggaagatgt tctgcggatc ccaccgcgct 14880 ttggcccgct gcagccgcgg gtagttgtct ttgtagtaca ggtcgtgcca ggcaacaccg 14940 gaggtgttcc acaatggatc ggccaagtcg gtgtccgggt agttgatgta ggagccgtcg 15000 acacgggtac ctggcaccgg aactccgccg gtttcggcgt acatctcgcg gtagaaaccg 15060 cgaatccagg tcagatgccg ctcgtcctcg gcgggctccg accagttcgt gacgaacagc 15120 gctttgagaa ccgagtcgcg ctgagcgagt gcggtggccg acggagccac ggcattcgcc 15180 ataccgccgt aaccgagcag caacagcgcc gccgcagggt tgtcgtatcc gtagacggtc 15240 agccgccggt aaaccgtggc tagttgagct tcggacagcc cggtgcgcaa gtaggcggct 15300 ttgaccttgg tccgttgcat gcccggttcg ccgccttcgg cgatcgcccc ggccacctgg 15360 gtcgatcgca accacggcag ggtttcccgc agcccttcgg ctggagtcac gccgacctgg 15420 gcgttgatcg ccgacaggtg ttcggccagg gtgcgttccg cgttcggatc cgtgccgtcc 15480 aggtgaacgt tcagcgtgac gtagccagct tgccggtgtg cgcagacgag cgtgctgaac 15540 aacccgagtt gcgtggattc aggcgcgctg tgctgctcgt accaattgcc gaagttctgt 15600 aggagcacgg cgaatgactg ctctgtcagt tcgtgccacg gccagtggaa cgatcggagc 15660 agcactgtcg cgggcggccg tggcaggagc tctgcggcgt cggtgctgac cacgtccggc 15720 gttcggagcc aaaacctggt gacgatcccg aagttgccgc caccgccacc ggtgtgcgcc 15780 caccacaagt cgtgaccggc gcccgtggag ttccggtcgg cctcgacgat gtgcacttca 15840 ccggcctggt cgaccacgac gacctcgacg ccttgaaggt agtcgacgac cgaaccgaat 15900 cggcgcgaca gcgggccgta tcccccgccg aggatgtgcc cgcctgcgcc caccccggga 15960 catgcgccgg tcgggatcgt cacgccccag ttcttgaaca gggttcggta cacctgcccg 16020 agggcggcgc ccgcctcgat cgcgaatgcc ccgcgcgtgc tgtcgtagta cacgcggttg 16080 agctcggaga ggtcgacgag cactcggatc gccgggtccg caacgagatt ctcgaagcag 16140 tgcccgccgc tgcggacccc tacccgcctg ccggtgcgca cggcgtcggc gacggcgtgc 16200 acgacgtctt cggcggagct ggcgatgtgg atgcgttcgg gttttccggt gaaacggggg 16260 ttgtgcccga cgacgaggtc cggataacga ggatcgtcgg gctcgacggt gatctctgtt 16320 cctggggttc gacgattcat gggtgccggg tcatggaatt cgggcaccgc ccctcctttt 16380 ctgactggtc cactttgttc gcccgcagcc gagatcatct acgcgtccgg gtgattatct 16440 gtgtgtttca gctcatacgt gaaacccggt cgcctccgcc ggctctactt tgtggatcga 16500 tatcgcggtg cgcatggtgc cgtatgcgct ggaaccgaaa aggtgatgac ttaccatgag 16560 tgagatcgca gttgccccct ggtcggtggt ggagcgtttg ctgctcgcgg cgggtgcggg 16620 cccggcgaag ctccaggaag cagtgcaggt ggccggactg gacgcggtgg ccgacgccat 16680 cgtcgacgaa ctcgtcgtac gctgcgatcc gctgtcgttg gacgagtcgg tgcgaatcgg 16740 cctggagatc acttctggcg ctcagctggt ccggagaacc gttgagctcg atcacgcagg 16800 cctgcggctc gcggcggtcg ccgaagcagc tgctgttctc cggttcgacg cggtggatct 16860 gctggaaggg ctcttcggcc cggttgacgg caggcggcac aacagccgtg aagtccgctg 16920 gtcggacagc atgacgcagt tctcgcccga ccagggcctc gccggcgcgc agcgcctgct 16980 ggcgttccgg aacagggtgt ccaccgcggt gcacgccgtg ctggccgcag ccgccaccag 17040 gcgcgcggac ctcggtgcgc tggcagtccg ctacggatcc gacaaatggg cggacctgca 17100 ctggtacacc gaacactacg agcaccactt ctcccgattc caggatgccc cggtgcgagt 17160 gttggaaata ggaatcggtg gttatcacgc acccgaactc ggtggtgctt cgctgcgcat 17220 gtggcagcgg tacttccggc gaggtctcgt ttacgggctg gacattttcg agaaagccgg 17280 gaacgaaggg caccgagtgc gaaagctgcg aggtgaccag agcgatgcgg aattcctgga 17340 agacatggtg gcgaagatcg gcccgttcga cattgtcatc gacgacggca gccatgtcaa 17400 cgaccacgtc aagaaatcct tccaatccct gtttccgcac gtccgcccag gtggtttgta 17460 cgtcatcgag gatctccaga cggcgtactg gcccggctac ggcggtcgcg atggggaacc 17520 cgcggcccag cgcacctcga tcgacatgct caaagaactg atcgacggcc tgcattatca 17580 ggagcgcgaa tcgcggtgcg ggaccgagcc ctcctacacg gaacggaacg tggcggccct 17640 gcacttctac cacaacctgg tattcgtgga gaaagggctc aacgctgaga ctgccgcgcc 17700 ggggttcgtg ccccggcaag cgctcggcgt cgagggcggc tgagccgttc accagctgcg 17760 gcgccagtag gcgcccgtgc cgtcgatgtc gtggatgggt tccgtgatcc cgagttccgc 17820 gcggaacccc ttcaccgcgt cctggcagga cggcagaaaa tagtcgtcga tgatgacgaa 17880 tccgcccggc gagagcttcg ggtacaggtt ccgcaatgag tccattgtgg attcgtagag 17940 gtcgccgtcg agtcgtagca cggcgagttc ctggatgggg gcggtgggca aggtgtcccg 18000 gaaccagccg gggaggaacc tgacctgttc gtcgagcagc ccgtagcggg cgaagttctg 18060 ccggacggtc tcaagcgata cgccaagcac gtcgttgtac tcgtgcagcg ccatagcctg 18120 gtccgcttgg tggtcttgcg cagagctttc cggcattccc tggaaggaat ccactaccca 18180 gacggtacgt ccggtatctc cgaatgcctg gagaaccgcg cgcatgaaga tgcatgcgcc 18240 gccccgccag acaccggtct cggcgaaatc cccgggaaca ccgtctgcga gcacggcttc 18300 cacgcagtgc tggaggttgt ccagccgctc cagaccgatc atcgtgtgcg cgacagttgg 18360 ccagtccgtg cctttggccc gagcggcctg cctgtagtcg gtgttgtcct gccaggcgtt 18420 cggatgcggc cgatcactgt aaatcgtgtt ggtgagtacc ttcttgagca ggtccaggta 18480 cagcgcgttc tgggagggca tcggttctcc ggatccagct gttctcgggt gactagttca 18540 tcaggcacgg atggccgcag tgttctccag tgtccgcacc agcgcggcgg gatggggcat 18600 ggccgtgatc tcgtcgctga gtttgattgc cgcagaagcg aagccggtgt cgccgagcac 18660 cgttgcgatt gagtcggtga actgttcgtg gtcggactgg gcctgctcat ccggcaagca 18720 gatgcccgcc ccggcagcgg cgaggttgcg cgcgtagtcg aactggtcga agtactgggg 18780 aagcacgagt tgcgggatgc cgagtcgggt cgcggtgaat gccgttcccg agccgcccgc 18840 gcagatgacc agctcgcagg tacgcaggaa caggttgagc gggaccgatt cggcgatccg 18900 ggcgttgtcg ggtaggtcgg tgagaagtgc ccggtgctcg gggggaacgg cgatcacggc 18960 ctcgacgccg ggcaactcgg tggcagccgc tactgcgcgc agcagcggag ccggcccggt 19020 ggcgttcagc accatgcggc ccatgcagat gcagacccgc cgtgctgagg tgcgcgccgc 19080 gccccatgcc gggaatgcgc cgcttccgtt gtacggcacg tactggaccg gtgcgccttg 19140 cggcgcgtcg cttgcttgca ggctcggcgg acagggatcg aggatgagct cgggagtggg 19200 caggccggtc agtccgtggt gccggcacac cgggtcaagc aactcgtggg ctcgatcgct 19260 gaaggggcct gcggtggggt cgactcccca gcggtgcagc acgaccggca ggtcgagcaa 19320 tccgccgagc acccggccga tcagcgcgca gacgtcgacc aacagcactg acggtcgcca 19380 ggcctcggcc agtcgaaggt attcggggag ctgatcgagc gagctttgcg cgacattgga 19440 cgcggtctgc tcccacagtt gccggcctgc ctcggtgtcg cgctgaccga acgccggatt 19500 gggaaagcgc agctgcgtgg ttccacccgt atcgccggtc ctgtcgttcc cgcggatccc 19560 ggccgtggtg agacctgcac catgcgcggt cgcctgcagc tctggtggtg cggcgatcag 19620 gacctcgtgc ccggatgctt gcagcgccca gcacagcggc accattgcca tgagatgcgt 19680 cggatagggc aagggaacga cgagtacgcg catacttcgg accccagtct ctttcccccg 19740 attagcgcag cagcccctac tcccattggc caggatttgg aaaatgcgct gcgtatgtcg 19800 atcgccgttg acgtccaacg gacttccggc ggcaacaata gtgtgtcacg gcaggaatgt 19860 cacgcgacca tcgaagatct ttgggtcgcc gcacctggtt tcacgcgaac gagtgaaatg 19920 cgcgagctcc gctcgatcgg ggtgggccgg acctgtacgg tgatcaccgt tggttctgcg 19980 gggattcatg gggaagattt gcgctggctg tttgcctcct ggccggatag ttatagtcgg 20040 taccgccgca tgcggcggta accgcgaatt aactgacggc tagtttgccg tcttttctct 20100 ctgtgtgttt cctgctcggt tccagaaaat tacgagaagg tgaacgttgc agagatcagg 20160 cataccggtg ttgccaggtg gcgcaccaac atcgcagcag gttgggcaga tgtatgacct 20220 ggtcacgccg ttgctgaact cggtcgcggg cggcccctgc gccatccacc acggctactg 20280 ggagaacgac gggcgggctt cctggcagca ggccgccgac cggctcaccg accttgtcgc 20340 cgaacggacc gtgctcgatg gcggcgttcg actgctcgat gtggggtgcg gtaccggaca 20400 accagcgctg cgcgtcgcgc gcgacaacgc gatccagatc accggcatca ccgtcagcca 20460 ggtgcaagtg gccatcgccg ctgattgcgc acgcgaacgc ggactaagcc accgggtgga 20520 cttctcgtgc gtcgatgcca tgtccctgcc gtacccggac aatgctttcg acgccgcctg 20580 ggccatgcag tcgctgttgg agatgtccga accggaccgt gccatccggg aaatccttcg 20640 agtactcaaa cccggtggca tcctcggcgt caccgaggtc gtcaaacgag aagcgggcgg 20700 cgggatgccg gtgtccgggg acaggtggcc gaccggcctt cggatctgcc tggctgagca 20760 acttctggaa tcgctgcgtg cagcggggtt cgagatcctc gattgggagg acgtgtcgtc 20820 gaggacccgg tacttcatgc cgcagttcgc cgaagagctc gctgcgcacc agcacgggat 20880 cgcggacagg tacgggccgg ctgtcgccgg ctgggccgcc gcggtctgcg attatgagaa 20940 atatgcccac gacatgggct atgcgattct gacggcgcgg aagccggtcg gctgagggcg 21000 cgccgcaatt cgatgacgtt catgcgccgt gtcggagaat cgccggtggc ggcgccagca 21060 gaggctgaac ttactggtgg tgtgtccagg aatcggaggg gcagtaccga atgagcgaag 21120 ccgggaacct gatagccgtc atcggactgt cctgccgcct accccaggcg cctgacccgg 21180 cttccttctg gcggttgctg cgcaccggaa cggacgccat caccacggtc ccggaagggc 21240 ggtggggcga cccgttgcct ggtcgggatg cgcccaaggg cccggaatgg ggtggtttcc 21300 tggctgatgt cgactgcttc gatcccgagt tcttcgggat ctcgccgcga gaagcggcaa 21360 ccgtggatcc ccagcagagg ctggctctgg agctcgcctg ggaggcactc gaagacgccg 21420 gtatccccgc cggcgagctg cgcggtactg ccgccggtgt gttcatgggg gcgatctctg 21480 acgactacgc cgccctgctg cgcgagagcc cgccggaagt ggctgcgcag taccgcctca 21540 ccggcaccca tcgaagcctg atcgccaacc gcgtgtccta tgtgctcggc ctgcgcgggc 21600 caagcctgac ggtggattca ggtcagtcct cgtccctggt cggcgtgcat ctcgccagcg 21660 agagcctgcg acggggtgag tgcacgatcg cactcgccgg cggcgtgaac ctcaacctgg 21720 ccgccgagag caacagcgct ctgatggact tcggcgcgct ctccccggac ggtcgctgct 21780 tcaccttcga tgtgcgggcg aacggttacg tccgtggtga gggcggcggc cttgtcgtgc 21840 tgaagaaggc cgatcaggcg cacgccgatg gcgaccggat ctactgcctc atccgcggca 21900 gcgcggtcaa caacgatggg ggcggtgccg ggctcaccgt tccggcggcg gacgcccagg 21960 cggagctgct gcgccaggca taccggaacg cgggcgtcga cccggccgcc gtgcagtatg 22020 tcgagctcca cggcagcgcg accagggtcg gggatcccgt cgaagcagca gccctcggag 22080 ctgtcctggg ggcggcgaga cggcccggcg acgagctgcg tgtggggtcg gcgaagacca 22140 acgtcggcca tctggaagca gcggcgggcg tcaccgggtt gctgaagacc gcactcagca 22200 tctggcaccg cgaactgccg ccgagtcttc atttcaccgc ccccaacccg gaaatcccgc 22260 tggacgaatt gaacctacgc gtccagcgtg atctgcggcc gtggccggag agcgaggggc 22320 cgctgctggc cggcgtcagc gccttcggaa tgggaggcac gaactgccac ctggtgctct 22380 ccggcacgtc ccgggtggag cgacggcgca gtggacccgc tgaggcgacc atgccgtggg 22440 tcttgtcggc cagaacaccg gtcgcattgc gtgcgcaggc ggcgcgcttg cacacgcacc 22500 tcaatacggc cggtcaaagt ccgttggacg tcgcctactc actggcgacc actcgatccg 22560 cgctaccgca ccgggccgcg ctggtcgcgg acgacgaacc gaaactgctc gccgggttga 22620 aggccctcgc tgacggcgac gacgcgccca cgctgtgcca cggcgcgact tccggcgagc 22680 gggcagcggt cttcgtcttt cccggacagg gcagccagtg gatcgggatg ggtaggcagc 22740 tgctcgaaac ctccgaggtt ttcgcggcgt cgatgtcgga ctgcgccgac gcattggcgc 22800 cacacctgga ttggtccctg ctggatgtgc tgcgcaacgc ggccggcgct gcgcaccttg 22860 accacgacga tgtcgtccag cccgcgctgt tcgccatcat ggtctcgctc gcggagctct 22920 ggcgttcgtg gggcgtgcgt ccggtggcgg tcgtcgggca ctcgcagggg gagatcgcgg 22980 cggcctgcgt cgccggggcc ctgtccgtcc gcgatgccgc cagggtggtg gcggtgcgca 23040 gcaggcttct gacggcgctg gccggcagtg gcgcgatggc ctcgttgcag catcccgccg 23100 aagaggtgcg gcaaatcctg ttgccctggc gcgatcggat cggcgtggcg ggggtgaacg 23160 gaccgtcgtc gaccctggtg tcaggggacc gggaggcgat ggcggaactg ctggccgagt 23220 gcgcagaccg agagctccgg atgcgccgga ttcccgttga atacgcctcc cattcgcctc 23280 acatcgaggt tgtccgggat gagctgctgg ggctgttggc gccggtcgaa cccaggacgg 23340 gaagcatccc gatctattcg acgacgaccg gggacctgct ggaccggccg atggacgccg 23400 actactggta ccgcaacctt cgtcaaccgg tgctgttcga agcggccgtc gaggccctgt 23460 tgaagcgggg gtacgacgca ttcatcgaga tcagcccaca cccggtgctg actgcgaaca 23520 tccaggaaac cgccgtgcga gcagggcggg aggtagtggc gctcgggaca ctccgccgcg 23580 gcgaaggtgg catgcggcag gcgctgacgt cgctggccag agcacacgta cacggagtgg 23640 ccgcggactg gcacgcggtc ttcgccggta ccggggcgca gcgggtcgac ctgccgacgt 23700 acgcctttca gcgacagcgc tactggctgg acgcgaagct tcccgacgtc gccatgcccg 23760 agagcgacgt gtcgacggcg ttgcgggaaa agctgcggtc ttcgccgagg gcggacgtgg 23820 actcgacgac cctcacgatg atccgggcac aggcagccgt ggtcctcggc cactccgatc 23880 cgaaagaggt ggacccggat cggacgttca aggacctggg cttcgattcc tcgatggtgg 23940 tcgagctgtg cgaccgccta aacgccgcca caggtctgcg actcgcaccg agcgtcgttt 24000 tcgactgtcc tacgccggac aagctcgccc gccaggtacg gacgttgttg ttgggcgagc 24060 cggctcccat gacgtcacac cggccggact ccgatgcgga cgagcctatc gccgtgatcg 24120 ggatgggctg tcggtttccg ggtggggtgt cctcgcccga ggagttgtgg cagttggtcg 24180 ccgctgggcg ggacgtcgtg tccgagttcc cggctgaccg aggttgggac ctggagcgtg 24240 cggggacatc gcacgtgcgc gccggcgggt tcttgcatgg cgccccggat tttgaccccg 24300 ggttcttccg gatttcgccg cgcgaggcgt tggcgatgga tccacagcag cggttgctgc 24360 tggaaatcgc ctgggaagca gtcgaacgag gcgggatcaa cccgcagcac ctgcacggaa 24420 gtcaaaccgg ggtcttcgtc ggcgcgacct ccctggacta cgggccacgc ctgcacgaag 24480 cgtccgagga ggcggccggg tacgtgctca ccggcagcac cacgagtgtg gcgtcgggtc 24540 gggttgcgta ttcgttcggg ttcgagggcc ctgcggtgac ggtggatacg gcgtgttcgt 24600 cgtcgttggt ggccctgcat ttggcgtgtc agtcgttgcg ttcgggtgag tgtgatctgg 24660 cgttggccgg tggtgtgacc gtgatggcca cgccggggat gttcgtggag ttttcgcggc 24720 agcgtggttt ggcgccggat gggcggtgca agtcgttcgc ggaggccgcc gacggcaccg 24780 gctggtccga gggtgctggc ctggttctac tggagcggtt gtcggatgcc cggcggaatg 24840 ggcatgaggt gctggcggtt gttcgtggta gtgcggtgaa tcaggacggt gcgtcgaatg 24900 gtttgaccgc gccgaatggt tcgtcgcagc agcgggtgat tgcccaggca ttggcgagtg 24960 cggggttgtc ggtgtccgat gtggatgctg tggaggcgca tgggacgggc acgcggcttg 25020 gtgatccgat cgaggcgcag gcgctgatcg ccacctacgg ccagggccgg cttccggaac 25080 ggccattgtg gttgggctcg atgaagtcga acatcggtca cgcgcaggca gctgcgggga 25140 tagccggcgt catgaagatg gtgatggcga tgcggcacgg gcagctaccg cgcacgttgc 25200 acgtggatga gccgacttct ggggtggatt ggtcggcggg gacggttcaa ctccttacgg 25260 agaacacgcc ctggcccggg agtggtcgtg ttcgtcgggt gggggtgtcg tcgttcggga 25320 tcagtggtac taacgcgcac gtcatcctcg aacagccccc gggagtgccg agtcagtctg 25380 cggggccggg ttcgggctct gtcgtggatg ttccggtggt gccgtggatg gtgtcgggca 25440 aaacacccga agcgctatcc gcgcaggcaa cggcgttgat gacctatctg gacgagcgac 25500 ctgatgtctc ctcgctggat gttgggtact cgctggcgtt gacacggtcg gcgctggatg 25560 agcgagcggt ggtgctgggg tcggaccgtg aaacgttgtt gtgcggtgtg aaagcgctgt 25620 ctgccggtca tgaggcttct gggttggtga ccggatctgt gggggctggg ggccgcatcg 25680 ggtttgtgtt ttccggtcag ggtggtcagt ggctggggat gggccggggg ctttaccggg 25740 cttttccggt gttcgctgct gcctttgacg aagcttgtgc cgagctggat gcgcatctgg 25800 gccaggaaat cggggttcgg gaggtggtgt ccggttcgga tgcgcagttg ctggatcgga 25860 cgttgtgggc gcagtcgggt ttgttcgcgt tgcaggtggg cttgctgaag ttgctggatt 25920 cgtggggggt tcggccgagt gtggtgttgg ggcattcggt gggcgagttg gcggcggcgt 25980 tcgcggcggg tgtggtgtcg ttgtcgggtg cggctcggtt ggtggcgggt cgtgcccggt 26040 tgatgcaggc gttgccgtct ggcggtggga tgctggcggt gcctgctggt gaggagctgt 26100 tgtggtcgtt gttggccgat cagggtgatc gtgtggggat cgccgcggtc aacgctgcgg 26160 ggtcggtggt gctctctggt gatcgggatg tgctcgatga ccttgccggt cggctggacg 26220 ggcaagggat ccggtcgagg tggttgcggg tgtcgcatgc gtttcattcg tatcggatgg 26280 atccgatgct ggcggagttc gccgaattgg cacgaaccgt ggattaccgg cgttgtgaag 26340 tgccgatcgt gtcgaccttg accggagacc tcgatgacgc tggcaggatg agcgggcccg 26400 actactgggt gcgtcaggtg cgagagccgg tccgcttcgc cgacggtgtc caggcgctgg 26460 tcgagcacga tgtggccacc gttgtcgagc tcggtccgga cggggcgttg tcggcgctga 26520 tccaggaatg tgtcgccgca tccgatcacg ccgggcggct gagcgcggtc ccggcgatgc 26580 gcaggaacca ggacgaggcg cagaaggtga tgacggccct ggcacacgtc cacgtacgtg 26640 gtggtgcggt ggactggcgg tcgttcttcg ccggtacaag ggcgaagcaa atcgagctgc 26700 ccacctacgc cttccaacga cagcggtact ggctgaacgc gctgcgtgaa tcttccgccg 26760 gcgacatggg caggcgtgtc gaagcgaagt tctggggcgc cgtcgagcac gaagatgtgg 26820 aatcgcttgc acgcgtattg ggcattgtgg acgacggcgc tgctgtggat tccctgagaa 26880 gcgcccttcc ggtgttggcc ggttggcagc gaacccgcac caccgagtcc attatggatc 26940 agcggtgtta ccgaattggc tggcggcagg tagccggact cccgccgatg ggaactgttt 27000 tcggtacctg gctggtcttc gcgcctcatg gctggtccag cgaaccggag gtggtggact 27060 gcgttacggc actgcgggca cgtggtgcct cggtggtgtt ggtggaagct gatcccgacc 27120 cgacctcctt cggcgaccgg gtacgaaccc tgtgttcggg ccttccggat cttgttggcg 27180 tgttgtcaat gttgtgcttg gaagaatcgg tccttccggg attttctgcg gtgtcacggg 27240 gttttgcgtt gaccgtggag ttggtgcggg ttttgcgggc agctggtgcg actgcccggt 27300 tgtggttgct gacgtgtggt ggcgtgtcgg tgggagatgt accggttcgt ccagcgcagg 27360 ccctggcgtg ggggttgggg cgtgttgtgg ggttggagca tccggactgg tggggcggct 27420 tgatcgatat tccggtcttg ttcgacgaag acgctcaaga gcggttgtcg attgtgctgg 27480 caggtctcga tgaggacgag gtcgcgatcc gtcctgacgg catgttcgcg cgtcggttgg 27540 tacgccacac tgtctcagct gatgtgaaga aggcgtggcg ccccagggga tcggtgctgg 27600 tgacgggcgg cacgggtggt ttgggggcgc acgttgctcg ctggctggcc gacgccggag 27660 ccgaacatgt ggcgatggtg agtcgacgcg gcgagcaggc accgagtgct gagaagttgc 27720 ggacggaact ggaggatctg ggtacccggg tgtcgatcgt gtcatgcgat gtgaccgatc 27780 gcgaggcgct cgccgaagtg ctgaaagccc ttccggctga aaacccgttg accgcggtag 27840 tgcatgcggc aggcgtgatc gagactggtg atgcggcggc aatgagcctg gctgatttcg 27900 atcacgtgtt gtccgcaaag gtggccggtg ccgcgaatct ggatgccttg ttggccgatg 27960 tggaattgga cgcgttcgtc ttgttctcat cggtgtcagg agtttggggc gctgggggac 28020 acggggctta cgcagcggcg aatgcctatc tggatgcgct cgcggaacag cgtcggtcgc 28080 gagggctggt cgcgactgcg gtggcctggg ggccgtgggc cggcgagggc atggcctccg 28140 gagaaacagg agaccagctg cgccgatacg gcctttcccc aatggctccg cagcacgcca 28200 tcgccggaat ccggcaggcc gtggaacagg acgaaatttc cctggtagtg gccgatgtcg 28260 attgggcacg tttcagcgcg ggattgctgg cggctaggcc gcggccgctg ctgaacgaac 28320 tggccgaggt caaggaactc ctcgtcgatg cccagcccga ggcgggagtc cttgccgacg 28380 cgtcgttgga atggcggcag cgattgtccg cggcaccgag gccgacacag gaacagctga 28440 tcctggagct ggtacgcggc gaaaccgctc tggtgctggg acaccccggg gcagcggccg 28500 ttgcatcgga acgagccttc aaggacagcg gattcgactc gcaggccgcg gtcgaactcc 28560 gcgttcggct caatcgagct accggcctcc agttgccatc gacaattatc ttcagccatc 28620 ccacgcctgc ggaactggct gcggagctgc gggcgaggct tcttcccgag tccgcaggag 28680 caggcattcc cgaggaggac gaggcgcgaa tcagagcggc actgacgtcg atcccgttcc 28740 cggccttgcg cgaggcaggc ttggtgagtc cgctgctcgc acttgccgga cacccggtcg 28800 actccggtat ctcctcggac gatgcggccg cgacctcgat cgatgcgatg gatgtagccg 28860 gcctcgtcga agcagcgctg ggcgaacgcg agtcctgaga ccgccgacct gggagatgac 28920 ggtgaccacc agttacgaag aagttgtcga ggcactgcga gcatcgctca aggagaacga 28980 acgcctccgg cgcggcaggg atcggttctc cgcggagaag gacgatccca tcgcgatcgt 29040 ggcgatgagt tgtcgttatc ccggtcaggt ctcctcgccg gaggacctgt ggcaactggc 29100 tgccggcggt gtggacgcga tctccgaagt tccgggggat cgcggatggg acctggatgg 29160 cgtgttcgtt ccggactccg atcgtcctgg cacgtcgtat gcctgcgcgg gcggttttct 29220 tcagggcgtg tcggagttcg acgcgggttt cttcgggatt tcgccgcgtg aggcgctggc 29280 gatggatccg cagcagcggt tgctgctgga agtcgcgtgg gaggtcttcg agcgggctgg 29340 gctggagcag cggtcgacac gcggttcccg cgttggcgtg ttcgtcggca ccaatggcca 29400 ggactacgcg tcgtggttgc ggacgccgcc gcctgcggtg gcaggtcatg tgctgacggg 29460 cggtgcggca gcggttcttt cgggccgggt tgcgtattcg ttcgggttcg agggtcctgc 29520 ggtgacggtg gatacggcgt gttcgtcgtc gttggtggcg ttgcacctgg cggggcaagc 29580 actgcgggcc ggtgagtgcg accttgccct tgccggtggc gtcacggtga tgtcgacgcc 29640 gaaggtgttc ctggagttct cccgccaacg gggtctcgcg ccggatgggc ggtgcaagtc 29700 gttcgcggcg ggtgcggatg gcactggatg gggtgagggt gccggactgt tgttgctgga 29760 gcggttgtcg gatgcccggc ggaatgggca tgaggtgctg gcggttgttc gtggtagtgc 29820 ggtgaatcag gacggtgcgt cgaatggttt gaccgcgccg aatggttcgt cgcagcagcg 29880 ggtgattacc caggcgttgg cgagtgcggg gttgtcggtg tccgatgtgg atgctgtgga 29940 ggcgcatggg acgggcacgc ggcttggtga tccgatcgag gcgcaggcgc tgatcgccac 30000 ctacggccgt gatcgtgatc ctggccggcc gttgtggttg gggtcggtca agtcgaacat 30060 cggtcatacg caagcggcgg cgggtgtggc tggtgtgatc aagatggtga tggcgatgcg 30120 gcacgggcag ctgccacgca cgttgcacgt ggaatcgccg tcgccggagg tggattggtc 30180 ggcggggacg gttcaactcc ttacggagaa cacgccctgg cccaggagtg gtcgtgttcg 30240 tcgggtgggg gtgtcgtcgt tcgggatcag tggtactaac gcgcacgtca tcctcgaaca 30300 gcccccggga gtgccgagtc agtctgcggg gccgggttcg ggttctgtcg tggatgttcc 30360 ggtggtgccg tggatggtgt cgggcaaaac acccgaagcg ctatccgcgc aggcaacggc 30420 gttgatgacc tatctggacg agcgacctga tgtctcctcg ctggatgttg ggtactcgct 30480 ggcgttgaca cggtcggcgc tggatgagcg agcggtggtg ctggggtcgg accgtgaaac 30540 gttgttgtgc ggtgtgaaag cgctgtctgc cggtcatgag gcttctgggt tggtgaccgg 30600 atctgtgggg gctgggggcc gcatcgggtt tgtgttttcc ggtcagggtg gtcagtggct 30660 ggggatgggc cgggggcttt accgggcttt tccggtgttc gctgctgcct ttgacgaagc 30720 ttgtgccgag ctggatgcac atctgggcca ggaaatcggg gttcgggagg tggtgtccgg 30780 ttcggatgcg cagttgctgg atcggacgtt gtgggcgcag tcgggtttgt tcgcgttgca 30840 ggtgggcttg ctgaagttgc tggattcgtg gggggttcgg ccgagtgtgg tgttggggca 30900 ttcggtgggc gagttggcgg cggcgttcgc ggcgggtgtg gtgtcgttgt cgggtgcggc 30960 tcggttggtg gcgggtcgtg cccggttgat gcaggcgttg ccgtctggcg gtgggatgct 31020 ggcggtgcct gctggtgagg agctgttgtg gtcgttgttg gccgatcagg gtgatcgtgt 31080 ggggatcgcc gcggtcaacg ctgcggggtc ggtggtgctc tctggtgatc gggatgtgct 31140 cgatgacctt gccggtcggc tggacgggca agggatccgg tcgaggtggt tgcgggtgtc 31200 gcatgcgttt cattcgtatc ggatggatcc gatgctggcg gagttcgccg aattggcacg 31260 aaccgtggat taccggcgtt gtgaagtgcc gatcgtgtcg accttgaccg gagacctcga 31320 tgacgctggc aggatgagcg ggcccgacta ctgggtgcgt caggtgcgag agccggtccg 31380 cttcgccgac ggtgtccagg cgctggtcga gcacgatgtg gccactgttg tcgagctcgg 31440 tccggacggg gcgttgtcgg cgctgatcca ggaatgtgtc gccgcatccg atcacgccgg 31500 gcggctgagc gcggtcccgg cgatgcgcag gaaccaggac gaggcgcaga aggtgatgac 31560 ggccctggca cacgtccacg tacgtggtgg tgcggtggac tggcggtcgt tcttcgccgg 31620 tacgggagcg aaacaaatcg agctgcccac ctacgccttc caacgacagc ggtactggct 31680 ggtgccatcg gattccggtg atgtgacagg tgccggtctg gccggggcgg agcatccgct 31740 gttgggtgct gtggtgccgg tcgcgggtgg tgacgaggtg ttgctgaccg gcaggatttc 31800 ggtgcggacg catccgtggc tggccgaaca ccgggtgctg ggtgaagtga tcgttgcggg 31860 caccgcgttg ctggagatcg ccttgcacgc gggggaacgt cttggttgtg aacgggtgga 31920 agagctcacc ctggaagcac cgctggtcct gccggagcgc ggggcgatcc aggttcagct 31980 gcgagtgggc gcgcccgaga attccggacg caggccgatg gcgctgtatt cacgccccga 32040 aggggcggcg gagcatgact ggacgcggca cgccacgggc cggttggcgc caggccgcgg 32100 cgaggcggct ggagacctgg ccgactggcc ggctcctggc gcgctgccgg tcgacctcga 32160 cgaattctat cgggacctcg cagagcttgg gctggagtac ggcccgatct tccaagggct 32220 caaggcggcc tggcggcaag gggacgaggt gtacgccgaa gccgcgctgc cgggaacgga 32280 agattctggt ttcggggtgc atccggcact gctggacgcg gctctgcacg caacggctgt 32340 ccgagacatg gatgacgcac gcttgccgtt ccagtgggaa ggtgtgtccc tgcacgccaa 32400 ggccgcgccg gctttgcggg tccgcgtggt cccggctggt gacgatgcca agtccctgct 32460 ggtttgtgat ggcaccggtc gaccggtgat ctcggtggac cgactcgtat tgcggtcggc 32520 tgcggcccgg cggaccggtg cgcgccgaca ggcccatcaa gctcggttgt accggttgag 32580 ctggccaacg gttcaactgc cgacatccgc tcagccaccg tcctgcgtgc ttctcggcac 32640 ctcagaagtg tccgctgaca tacaggtgta tccggacctc cggtcgttga cggctgcgtt 32700 ggatgccggt gccgaaccac ccggcgtcgt catcgcaccc acgccccccg gcggtggacg 32760 aacagcggat gtccgggaga cgactcggca tgcactcgac ctggtacaag gctggctttc 32820 cgatcagcga ctcaacgaat cccgattgct cctggtgaca cagggagcag tggccgtgga 32880 gccgggcgaa cccgtgaccg atctggcgca ggccgcgctc tggggactgc tgcggtcgac 32940 gcagaccgaa caccctgatc gcttcgtcct cgtcgatgtg cctgagcccg cgcaactcct 33000 ccccgcgctg ccgggggtgc tggcctgcgg cgaacctcag ctcgcgttgc gacgtggcgg 33060 cgctcatgcg cccagactgg ctggactggg cagcgatgac gtcctgcccg tgccggacgg 33120 caccgggtgg cgattggagg ccacgcgccc gggaagcctg gatgggttgg cattggtgga 33180 cgaaccgacg gccacggcac cgctgggtga cggtgaggtc aggattgcga tgcgcgcggc 33240 cggggtgaac ttccgggatg cgctcatcgc gctcggtatg tatcccggtg tggcatcgct 33300 gggcagtgag ggcgccgggg tcgtggtgga gaccggcccc ggcgtcaccg gcctggcacc 33360 cggcgaccgc gtgatgggaa tgatcccgaa ggcgttcggg ccgctcgcgg tcgccgacca 33420 tcgcatggtg acgaggattc ccgctggttg gagcttcgcg cgggccgcat cggtgccgat 33480 cgtctttctc accgcctact acgcgctggt tgatctcgcc gggttgagac caggggagtc 33540 gttgctggtt cattcggccg ccggtggggt ggggatggcc gcgatccaac tcgccaggca 33600 cctcggtgca gaggtgtacg ccaccgctag cgaggacaag tggcaagccg tggagctgag 33660 ccgagaacac ctcgcttcgt cgcggacgtg cgatttcgag cagcagttcc tcggggcaac 33720 cggcggacgc ggcgtcgacg tcgtgctcaa ctccctcgcc ggggagttcg ccgatgcgtc 33780 tctgcgaatg ctgccgcgcg gtggccgttt cctggagttg gggaagacgg atgttcgtga 33840 ccccgtcgag gtcgccgatg cgcatccggg cgtgtcttac caggctttcg ataccgtaga 33900 ggcaggcccg cagcgaatcg gcgagatgct tcacgagctg gtggagttgt tcgagggacg 33960 cgtgctggag cccctgcctg tcacggcttg ggacgttcgg caggcgcccg aggcgctacg 34020 gcacctgagc caagcgcggc atgtgggaaa gctggtgctc accatgcctc cggtgtggga 34080 cgccgcaggc acggttctgg ttaccggcgg aacgggagca cttggcgcag aggtcgcccg 34140 gcacctcgtg atcgagcgcg gggtgcgaaa cctggtcctc gtcagcaggc gcggtcccgc 34200 agccagtggc gctgctgagc tcgtggcgca actgacggcc tacggtgccg aggtttcctt 34260 gcaggcttgc gatgtcgccg atcgtgagac cttggcgaag gtgcttgcca gcatcccgga 34320 cgagcatccg ttgaccgccg tggtgcacgc ggctggtgtt ctcgacgacg gagtgtccga 34380 atcgctcacc gtggagcggc tggaccaggt tctgcgcccg aaggtcgatg gcgcgcggaa 34440 tctgctcgag ctgatcgacc cggacgtggc cctcgtgttg ttctcgtcgg tgtcgggtgt 34500 gctcggcagc ggtgggcagg gtaactacgc ggcggccaac tccttcctcg acgcattggc 34560 gcagcaaagg cagtcgcgcg gcctaccgac gagatcattg gcctgggggc cctgggcgga 34620 acatggcatg gccagcacct tgcgcgaagc cgagcaggat cgattggcgc gatctgggtt 34680 gctgccgatc tcgaccgagg aggggttgtc ccagttcgac gccgcgtgcg gcggcgcgca 34740 taccgtggtg gcgccggttc gattcagccg cttgtccgac gggaacgcga tcaagttctc 34800 cgtcctgcaa ggtttggtcg ggccgcatcg cgtcaacaaa gcggcgactg cggatgatgc 34860 cgagagcctc cggaaacggt tgggacgctt gccggatgca gaacaacatc ggattctgct 34920 ggacctcgtc cgcatgcatg tggcggcagt gctcggattc gccggttctc aggagatcac 34980 cgcggacggc acgttcaagg tgctgggctt cgactcgttg accgtggtcg agttgcgcaa 35040 ccggatcaac ggggcgacgg ggctgcgact gcccgccacc ctggtgttca actacccgac 35100 gccggatgcg ctcgccgcgc acctcgtcac cgcgctgtcc gcagaccgcc tggccgggac 35160 attcgaggaa ctcgacaggt gggcggcgaa cctgcccacg ctggccaggg atgaggccac 35220 gcgggcgcag atcaccaccc ggctacaggc gatcttgcag agcctggcgg acgtgtccgg 35280 cggaaccggc ggcggctccg tgccggaccg gctcagatcg gccacggacg acgagctttt 35340 ccaactcctc gacaacgatc tcgaacttcc ctgatgcctc agccggagcc ttcgcaactt 35400 cctggaggga aacgccacat gtcgaatgaa gagaagctcc gggagtactt gcggcgtgcg 35460 ctcgtggatc tgcaccaggc gcgcgagcgg ctgcacgagg cggagtcggg agagcgggaa 35520 cccatcgcga tcgtggcgat gggctgccgg tacccgggtg gggtgcagga cccggaaggg 35580 ctgtggaaac tggtcgcctc cggtggcgac gccatcggtg aattccccgc tgatcgtggt 35640 tggcacctcg acgagctcta cgatcccgac ccggatcagc ccggaacctg ctacacccgg 35700 cacggcggct tcctccacga cgccggcgag ttcgacgcgg gattcttcga catcagcccc 35760 cgtgaggcgc tcgcgatgga cccgcagcag cggctgctgc tggaaatctc ctgggagacc 35820 gtcgaatccg ctgggatgga cccgaggtcc ttgcggggga gccgcaccgg ggtgttcgcg 35880 ggattgatgt acgagggcta tgacaccggc gcccaccggg caggagaagg tgtcgaaggc 35940 tatctcggaa ccggcaatgc gggaagcgtc gcctctggtc gggttgcgta tgcgttcggg 36000 ttcgagggcc cagcggtgac ggtagacacg gcgtgctcgt cgtcgttggt ggcgctgcat 36060 ttggcgtgtc agtcgttgcg gcagggcgag tgtgatctgg cgctggccgg tggagtgacg 36120 gtgatgtcga cgccggagag gttcgtggag ttctcccgtc agcgtggtct cgcaccggat 36180 gggcggtgta agtcgttcgc ggcggctgcg gatggaaccg gttggggtga gggtgccggt 36240 ttggtgttgc tggagcggct gtcagacgcc aggcggaacg ggcatcgggt actggcggtt 36300 gttcgtggta gcgcggtgaa tcaggacggt gcgtcgaacg gattgacggc cccgaacggg 36360 ctggcccagg agcgggtcat tcagcaggtg ctcacgagtg cggggctgtc ggcgtccgat 36420 gtggacgctg tggaggcgca tggaacgggt acgcggcttg gtgatccgat cgaggcgcag 36480 gctctgatag ccgcctatgg acaggatcgg gaccgggacc ggccgctgtg gttggggtcg 36540 gtcaagtcca acatcggtca tacgcaggcg gctgcgggcg tcgctggtgt gatcaagatg 36600 gtcatggcga tgcggcacgg ggagctgccg cgcacgttgc acgtggacga gccgaattcg 36660 cacgtggact ggtcggctgg tgcggtccga ctcctgaccg agaacatccg ctggccaggg 36720 acgggtacgc gccgcgctgg agtgtcgtcg ttcggggtaa gcggtaccaa cgcacacgtc 36780 atcctcgaac acgacccgct cgccgtgacc gagaacgagg aagcagcgca gtccccagca 36840 cctgggatcg tgccctgggc gttgtccggg cggtcgtcga cggcgctgcg ggcccaggcc 36900 gaacggctgc gcgagctgtg cgagcagacc gatcccgacc ccgtcgatgt cggtttctca 36960 ctggccgcca cgcgcacggc ttgggagcac cgagcggtgg tgcttggtcg ggacagcgct 37020 acgttgcgct ccgggcttgg cgttgttgcc agcggtgaac cagcggtcga tgtcgttgag 37080 gggagcgtcc tggacggcga ggtcgtcttc gtcttccccg gtcagggctg gcagtgggcc 37140 ggtatggcag tcgacctgct ggacgcttcg ccgacgttcg cgcgccacat ggacgagtgc 37200 gccaccgcgc tgcggaggta cgtggactgg tcgttggtcg acgtgctgcg cggagcggag 37260 aactccccac cgctggaccg ggtggacgtg ctccagcccg cgtccttcgc ggtgatggtg 37320 tcgctcgccg aggtgtggcg ttcctacggg gtgaggccgg cggccgtcgt cggccacagt 37380 caaggcgaaa tcgccgcggc ctgcgcagcc ggggtgctgc cgctggagga tgcggccagg 37440 cttgtcgcat tgcgcagcag agcgttgaag ggactttcgg ggcggggtgg catggcgtcg 37500 ctggcctgcc ctgcggatga ggtcgcggca ttgttcgcgg gatcgggcgg ccgtctggaa 37560 gttgcggcga tcaacggccc gcgatcggtc gtggtgtccg gcgatctgga agcggtggac 37620 gaactgctgg cagagtgcgc tgaaaaggac atgcgtgcac gccgtatccc cgtcgactac 37680 gcctcgcatt cagcgcacgt ggaggtggtt cggagcccgg tgctggcggc cgccgccggg 37740 gtgcgacacc gggacggcca ggtgccgtgg tggtcgacgg tgatcggcga ctgggtggat 37800 ccggccaggc tggacggcga gtattggtat cggaacctcc ggcagccggt ccggttcgaa 37860 cacgccgtgc agggcctggt cgagcgggga ttcggcctgt tcatcgaaat gagtgcgcat 37920 ccggtgctga ccacggcggt cgaggaaacc ggtgcggagt cggagaccgc cgtggccgcg 37980 gtaggtacct tgcgacgtga ctcgggcggc ctccggaggt tgttgcattc gctggccgag 38040 gcgtacgtgc gcggcgccac cgtggactgg gccgtggcgt tcgggggcgc gggccgacgg 38100 ctggacctgc cgacctaccc gttccagcgc cagcggtact ggctggacaa gggagctgcc 38160 tccgacgagg ctcgtgcggt ctcggacccg gcggcgggct ggttctggca agccgtggcg 38220 cgccaagacc tgaaaagcgt gtccgatgcc ctcgatctcg acgccgacgc accgctgagc 38280 gcaacacttc cagccctgtc cgtctggcac cgtcaggaac gagaaagggt cttggcagac 38340 ggttggcggt accgagtcga ctgggtacgg gtggccccgc agccggtccg gagaacgcgg 38400 gaaacctggc tcctggtcgt tcccccgggc ggcatcgagg aagcgctggt cgaacggctg 38460 acggatgcgt tgaacacgcg agggatcagc accctgcgcc tcgacgtgcc accggcggcg 38520 accagtggcg aactcgcaac cgaactccgc gccgcagccg acggtgaccc ggtgaaggca 38580 atcctgtcgc tcaccgcgtt ggacgagcga ccccaccccg aatgcaagga cgtcccgagc 38640 gggattgcct tgctgctgaa cctggtcaag gcgctcggtg aagccgacct cagaattcct 38700 ctgtggacca tcacgcgtgg tgcggtcaag gcaggccccg cagatcggct gctgcgcccg 38760 atgcaggcgc aagcatgggg tctggggcga gtagccgcac tcgaacaccc cgagcgctgg 38820 ggtgggctga tcgacctgcc ggattcgctg gacggcgacg tcctcacgag gctgggcgaa 38880 gcgctcacca acggcttggc ggaagaccaa ctggcgattc gccagtcggg cgtgctggcc 38940 cggcgactgg tacccgcccc ggcgaatcag cccgctggac gtaagtggcg cccccgaggg 39000 agcgcgctga tcacgggcgg actcggcgcg gtgggcgcac aggtggcgag gtggttggcc 39060 gaaatcggag ccgagcgaat cgtgctcacc agtcgacggg gcaaccaagc agcaggcgcc 39120 gccgagctgg aagccgaact ccgggccctt ggagcgcaag tgtccatcgt ggcttgcgac 39180 gtgaccgatc gtgccgagat gtccgcacta ctggccgagt tcgacgtcac cgcggtgttc 39240 cacgcggccg gagtcggtcg gctgctgccg ttggcggaga ccgaccagaa cggcctggcc 39300 gaaatatgcg cggcgaaggt ccgcggcgct caggtgctgg acgaactgtg cgacagcacc 39360 gatctcgatg ccttcgtcct gttctcctcg ggtgccgggg tatggggcgg gggcggtcag 39420 ggcgcttacg gcgcggcgaa cgcattcttg gacacactcg ccgaacaacg ccgagcacgc 39480 ggtctgccgg caacctcgat ctcctggggc agttgggccg gcggcggcat ggccgacggc 39540 gcggcgggcg aacacctgcg gcgacgcggg atacgtccga tgccggcggc gtcggccatc 39600 ctggctctgc aggaagtact tgaccaggat gagacgtgcg tgtcgatcgc tgatgtggac 39660 tgggaccgat tcgttcccac gttcgccgcg actcgcgcca cccggttgtt cgacgaagtg 39720 ccggcggcga gaaaggcgat gcccgcgaat gggccggcag aaccaggcgg ctcgccgttc 39780 gcccgcaatc tcgcggagct gccggaagcc caacgacgcc acgaactggt ggatctggtg 39840 tgcgcccagg tggcaaccgt gctcgggcac ggcagtcgcg aggaagtcca gcccgagcgg 39900 gcgttccgcg cgctcgggtt cgactccctc atggcggtgg atctgcgcaa tcgtttgacc 39960 accgccaccg ggttgcgcct gccgaccaca accgtcttcg 40000 actacccgaa tccggccgcc ttggccgctc acctgctcga ggagctggtg ggtgatgtcg 40060 cgtcggctgc ggtgaccgct gccagcgcgc ccgcgagtga cgaaccgatc gcgatcgtcg 40120 cgatgagctg ccggtttccg ggtggcgcgc actcgccgga agacctgtgg cggctggtcg 40180 ccgccggcac ggaggtgatc ggcgagttcc cctccgaccg gggctgggat gcggaaggcc 40240 tttacgatcc ggatgcttcc aggcctggaa cgacgtatgc gcggatggcg ggattcctct 40300 acgacgccgg tgagttcgat gccgacctgt tcggcatcag cccacgtgag gcgttggcga 40360 tggatccgca gcagcggttg gtgctcgaaa tcgcctggga agccctcgaa cgggccggaa 40420 tcgatccgtt gtccttgaag ggcagtgggg tcggcacgta catcggcgct ggaagccgtg 40480 ggtacgcgac ggatgtgcgg cagtttcccg aggaggcgga gggctacctg ctgacgggta 40540 cctcggccag tgtgctgtcg ggtcgggtcg cgtattcgtt tggtttcgag ggtcctgcgg 40600 tgacggtgga tacggcttgt tcgtcgtcgt tggtggcgtt gcatctggcg tgccagtcgt 40660 tgcgttcggg cgagtgtgat ctggcgttgg ccggtggtgt gaccgtgatg tcgacgccgg 40720 agatgttcgt ggagttctcc cgtcagcgcg gtttggcgcc ggatgggcgg tgcaagtcgt 40780 tcgcggagag cgcggacggc accggctggg gcgaaggcgc gggcctgttg ttgctggagc 40840 ggttgtcgga cgcccaccgg aatgggcatc gggtgttggc ggtggttcgt gggtcagcgg 40900 tgaatcagga cggcgcctcg aacggactgg cggcgccgaa cggtccgtcg cagcagcggg 40960 tgatcaacca ggcactcgcg aatgcggctc tttcggcgtc cgatgtggat gcggtggagg 41020 cacatggcac cgggaccagg ctgggtgatc cgatcgaggc gcaggcattg atcgcaacgt 41080 atgggcaggc ccgggagcgg gatcggccct tgtggctggg gtcggtcaag tcgaacatcg 41140 gtcatacgca ggccgcggcg ggtgttgccg gtgtgatcaa gatggtgatg gccatgcggc 41200 acgggcagct gcccgcctcg ctgcacgcgg atgagcccac gtcggaggtc gattggtcgt 41260 cgggggcggt ccggctcctc gccgaacagg taccttggcc ggagtctgac cgtgttcgtc 41320 gggtgggggt ttcgtcgttc gggatcagcg gcaccaacgc acatgtgatc ctcgaacaag 41380 ctacgaatgc gccagatagt acagcggaga cggacaaaac agaatccgga tctactgtcg 41440 atattccggt cgttccctgg ttggtgtcgg gaaagacgac ggattccctg cggggacaag 41500 ccgaacgagt cttgtctcag gtcgagtccc ggccggagca gcgttcgctg gatgttgcct 41560 actcgcttgc ttctggccga gccgcgctgg atgaacgcgc tgtcgtgctg ggtgcggacc 41620 gcggtgagct ggttgctgga ctggcggcgt tggccgccgg tcaggaggct tctggggtga 41680 tcagcggaac tcgtgcttct gctcggttcg ggttcgtgtt ctcggggcag ggtggtcagt 41740 ggttggggat gggcagagcg ctctactcga agtttccggt gttcgctgct gcgtttgatg 41800 aggcttgcgc cgagttggag gcacatctgg gggaagaccg ccgggttcgg gatgtggtct 41860 tcggttccga tgcgcagctg ctggatcaga cgctgtgggc gcagtcgggt ctgttcgcgc 41920 tgcaagccgg cctcttgggg ctgctgggtt cgtggggcgt tcggccggat gtggtgatgg 41980 ggcattcggt cggggagttg gccgccgcgt ttgcggctgg cgtgttgtcg ttgcgggatg 42040 cggctcggtt ggtggccgcg cgcgcccggt tgatgcaagc cctgccctct gacggcgcga 42100 tgttggcggt ggctgctggt gaagaccttg ttcggccatt gctggccggt cgggaggagt 42160 ccgtgagcgt cgccgcgctc aatgcccccg gttcggtggt gttgtcgggc gatcgggagg 42220 tgctggccag catcgtcggc cggctgaccg agctccgagt ccggacgcgg cgcttgcggg 42280 tctcccatgc ttttcattcg caccggatgg acccgatgtt gggcgagttc gcccagatcg 42340 ccgagtctgc ggagttcggt aagccaacga caccgcttgt gtcgacgttg acgggtgagc 42400 tcgacagagc cgcggaaatg agcacaccag ggtattgggt gcgccaggcg cgtgaacccg 42460 tccgtttcgc cgacggtgtc caggccctgg cagcgcaggg cataggcacg gtcgtcgagc 42520 tcggcccgga cggaacgctg gcggcactgg ttcgggagtg tgcgaccgag tccgatcggg 42580 ttgggcggat ttcgtcgatc ccactgatgc gcagggagcg ggacgagacc cgttcggtga 42640 tgacagccct ggcgcatctc cacacccgtg gtggtgaggt ggactggcag gcgtttttcg 42700 ccggtaccgg cgctaggcag ctcgagttgc caacgtatgc cttccaacga cagcactact 42760 ggatcgagtc cagtgcgcgg ccagcacgcg accgcgcaga catcggcgag gtggcggaac 42820 agttctggac cgcggttgac caaggcgatc tggcaacgtt ggtcgccgct ctggatcttg 42880 gggcggacga cgacacatgc gcatcgttga gcgatgtatt gccggcgttg tcctcctggc 42940 gaagcggact ccgcaaccgt tcgctcgtcg attcctgccg gtaccgaatc agttggcatt 43000 cctctcggga ggtgccggcc ccgaagattt ccggtacctg gctgttggtc gtgcccggtg 43060 ctgcggatga cggattggtc acggctttga cgagttcact ggtcggaggc ggcgccgagg 43120 tcgtccggat cggcctgtcc gaagaggacc cgcaccgcga ggacgtcgca cagcggctgg 43180 ccaatgcgct gacggatgcc ggtcaactcg gtggcgtgct ttcgctgttg gggctcgatg 43240 aatcgcctgc tccgggattc tcctgcttgc caactggttt cgcgctgact gtgcagcttc 43300 tgcgggcctt gcggaaggcc gacgtcgagg cgcctttttg ggcggtgacg cgcggcggcg 43360 tcgcgttgga agatgtacgc gtgtctccgg agcaggccct ggtctggggg ctgctgcgtg 43420 tcgcgggact ggagcacccg gagttctggg gtggcttgat cgacctgcca tcggactggg 43480 acgaccgatt gggtgcccgg ttggcgggtg tgttggcgga tggtggcgag gatcaagtcg 43540 ccattcgccg tggtggtgtg ttcgtgcggc ggttggaacg cgctggtgcg tcgggtgccg 43600 ggtcggtgtg gcgtcctcgg gggacggtgt tggtgacggg tggtacgggc ggtttggggg 43660 cgcatgttgc ccggtggttg gccggtgccg gggctgagca cgtggtgttg accagccgtc 43720 gaggagcgga cgctccgggc gctggggaat tgcgggcgga gctggaggcg ctgggtgctc 43780 gggtgtcgat tgtgccctgc gacgtggctg atcgtgacgc agtggctgga gtgttggcag 43840 ggatcggtgg ggagtgtccg ctgactgcgg tggtacacgc cgccggggtc ggcgaggcgg 43900 gcgacgtagt ggagatgggt ttggcggatt ttgcagcggt gttgtcggcg aaggtgcgtg 43960 gtgcggcgaa tctggacgag ttgctggccg actcggagct ggatgcgttt gtgatgttct 44020 cctcggtgtc gggggtgtgg ggagccggcg gacagggtgc gtatgcggct gcgaacgcct 44080 acttggatgc gttggccgag cagcgtcggg cgaggggatt ggtcgggacc gcggttgcgt 44140 ggggaccgtg ggccggtgac ggcatggccg ccggcgaaac cggcgcacag ctgcaccgga 44200 tgggcctggc gtcgatggaa ccgagcgcgg cgctgctggc acttcagggt gcattggacc 44260 gcgatgagac ctccctcgtc gtggccgatg tcgattgggc acggttcgcc ccagccttca 44320 cctcggcacg tcgacgcccg ctgctggaca ccatcgacga ggcccgagcc gcattggaaa 44380 ccaccggcga acaagcgggc acaggcaaac ccgttgagct gacgcaacgc ctggccggac 44440 tgtcgcggaa ggaacgcgac gatgcggtat tggatctggt gcgggcggag acggcggctg 44500 tgctgggacg cgacgatgcc acggccctgg cgccatcgcg gccgttccag gaactcggat 44560 tcgactcctt gatggcggtg gagctgcgca accggctgaa caccgccacc gggatccagc 44620 tgcccgccag cacgattttc gactacccca atgccgagtc gctgtcgcgt cacctctgcg 44680 ccgagctttt cccaacggag actaccgtgg actcggccct tgccgagctc gatcgaatcg 44740 agcagcagct ctcgatgctc accggcgaag cgcgggcacg ggaccgaatc gcgacacgac 44800 tgcgagccct ccacgagaag tggaacagcg cagctgaagt accgaccgga gccgatgtcc 44860 tgagcacgct cgattcggcg acgcacgacg agatattcga gttcatcgac aacgagctcg 44920 acctgtcctg agcagttcct gcggaacttc aagcgccgaa atcgggtgga aatcacaatg 44980 gccaatgaag aaaagctctt cggctatctg aagaaggtaa ctgcggacct gcatcagacc 45040 cggcagcgcc tgctcgcggc cgagagccgg agtcaggagc cgatcgcgat cgtctcggcg 45100 agctgccgac tgcccggcgg cgtcgactct cccgaagcgc tctggcaact cgtgcgcact 45160 ggcaccgacg ccatctcgga gttccccgcc gaccggggct gggatctcgg ccggttgtac 45220 gatcccgacc cgaaccacca gggaacgtcg tacacgcggg ccggcggttt cctcgcagga 45280 gcgggcgatt tcgaccccgc catgttcggg atttcgccgc gtgaggcgtt ggcgatggac 45340 ccgcagcaac ggttgttgct ggagctgtcc tgggaggccc tcgaacgggc gggcatagac 45400 ccgacatccc tgcgcggcag caagaccggt gtcttcggtg gtgtcacgcc ccaggagtac 45460 gggccgtcct tgcaggagat gagccgaaac gctgggggtt ttggactcac cgggcggatg 45520 gtgagtgtgg cgtcgggtcg ggttgcgtat tcgtttggtt ttgagggtcc tgcggtgacg 45580 gtggatacgg cgtgttcgtc gtcgttggtg gccctgcatt tggcgtgtca gtcgttgcgt 45640 tccggcgaat gcgatctcgc gctggccggc ggtgtgacgg tgatggcgac accggcgacg 45700 ttcgtggagt tctcccgtca gcgtggtttg gctccggacg ggcggtgcaa gtcgttcgcg 45760 gctgccgcgg atggcaccgg gtggggtgag ggtgccggtc tggtgttgct ggagcggttg 45820 tcggatgcgc ggcggaatgg gcacgaggtt ctggcggtgg tgcggggtag cgcggtgaac 45880 caggacggcg cgtcgaatgg tttgactgcg ccgaatggtc cgtcgcagca gcgggtgatc 45940 acccaggcgt tggcgagtgc ggggctgtcg gtttccgatg tggatgcggt cgaggcacat 46000 gggaccggga ccacgttggg tgatccgatc gaggcacagg ccctgatcgc cacgtacggg 46060 cagggccggg agaaggatcg gccgttgtgg ttggggtcgg tcaagtccaa catcggtcac 46120 acgcaggcgg ccgctggcgt tgccggcgtc atcaagatgg tcttggcgat gcggcacggg 46180 cagctgcccg ccacgttgca tgtggatgag cccacgtcgg cggtggactg gtcggcgggt 46240 tcggtccggc ttctcacgga gaacacgccc tggccggaca gtggtcgtcc ttgccgggtg 46300 ggggtgtcgt cgttcgggat cagcggcacc aacgcacatg tgattctcga acagtctcca 46360 gtcgagcagg gcgaaccggc cgggccggtc gaaggcgagc gggaaccgga tgtagccgtc 46420 cccgtggtgc cttgggtgct gtcgggtaag acaccggagg ctgcgcgggc gcaggccgaa 46480 cgggtgcatt cgcatatcga ggaccggccg gggctgtcgc cggtggatgt ggcgtattcg 46540 ctaggaatga cacgcgcggc gctggatgaa cgcgcagtgg tgttgggctc ggaccgtgcc 46600 gcgctcctga ccgggttgag ggcattcgcc gacggctgcg atgcgcccga agtggtttcg 46660 gggtctgtgg ggcttggtgg ccgcgtcggg ttcgtgttct cgggtcaggg tggtcagtgg 46720 ccggggatgg gccgggggct ctactcggtg tttccggtgt tcgccgacgc gttcgacgag 46780 gcttgcgcgg agttggatgc acacctgggc caggaactgc gggttcggga tgtggtgttc 46840 ggttcgcaag cgtggttgct ggatcggacg gtgtgggcgc agtcgggttt gttcgcgttg 46900 cagattggct tgctgcggct gctgggttcg tggggtgttc ggccggatgt ggtgttgggg 46960 cactcggtgg gtgagctggc tgcggtgcat gcggctggtg tgttgtcgtt gtcggaggcc 47020 gcgcggttgg tggcgggtcg cgcccggttg atgcaggcgt tgccttctgg tggtgccatg 47080 ctcgcggtcg ctacgggtga gtttcaggtc gatcctctgc tggatggggt gcgggaccgg 47140 atcggtatcg cggcggtgaa tggcccggaa tcggttgtgc tctctggtga ccgcgagctg 47200 ctcaccgaga tcgctgatcg gttgcacgat caggggtgcc ggacccggtg gttgcgggtg 47260 tcgcatgctt tccattcgcc ccatatggag ccgatgctgg aggagttcgc ccagatctcc 47320 cgaggccgcg aatatcacgc accggaactg ccgatcatct cgaccctgat cggtgagctg 47380 gacggtggtc gagtgatggg cactcccgag tactgggtgc gtcaggtgcg tgagcccgtc 47440 cgtttcgccg agggtgtcca ggcgcttgtc ggtcagggtg tcggcacgat tgtcgaattg 47500 ggtccggacg gggcgttgtc gacgttggtc gaggagtgtg tggcggaatc cgggcgggtg 47560 gccgggatcc cgctgatgcg caaggaccgc gacgaggcgc gaaccgtgct ggcagctttg 47620 gcgcagatcc acacccgtgg tggtgaggtg gactggcggt cgtttttcgc cggtaccggg 47680 gcgaagcaag tcgacctgcc cacctacgcc ttccagcggc agcggtactg gctggcatcc 47740 accgggcgtg cgggtgacgt gaccgccgcc ggattggccg aggcggacca tccgctgctc 47800 ggtgcggtgg ttgcgttggc agacggcgaa ggtgtggtgc tgaccggtcg gttgacagcg 47860 ggttcgcatc cgtggttgtc cgatcaccgg gtgctgggcg aaatcgtcgt ccccggcacc 47920 gcgatcgtcg agctggtgtg gcacgtcggc gagcgcctcg gttgtggccg ggtggaagaa 47980 ctggctttgg aagcgcccct gatcctgccg gatcatggag cggtccaggt tcaggtgctg 48040 gtgggaccgc ccggggaatc cggagcccgg tcggtggcgc tctactcctg tcctggcgag 48100 gcgatcgaac ccgagtggaa gaagcacgcg acgggcgtgc ttctcccacc cgtggccgcc 48160 gagaaccatg agctgaccgc atggcccccg gagaatgcga ccgaaatcga tgcagacggg 48220 gtctacgcat tccttgaagg gcacggtttc gcgtacggac cggcctttag atgtctgcgc 48280 ggtgcctggc gacgaggcgg ggaggtgttc gccgaagtcg cattgccgga tgacatgcag 48340 gcgggggtcg atcgattcgg cgtccacccc gcgttgctgg acgcggttct gcatgccgcc 48400 gcagccgaga cgtcggtggt ccagagcgaa gcgcgggtgc cgttctcgtg gcgtggggtg 48460 gaacttcgcg ccactgaaag cgcggtggtg cgggcgcgcc tctcgttgac ttcggatgac 48520 gaactgtcgt tggtcgcagt ggacccggct ggccgattcg tggccacggt tgattcgctg 48580 gtgacccgac cgatctcccg gcagcaggtg aggtctggcg cgatcggtga ttgcctgttc 48640 gaggtggagt ggcaccggaa ggcgttgttg ggaacaaccg ccggcgacga ccttgccatc 48700 gtcggtgacg gtcccagttg gccggaatcg gtgcgcgcaa ccgcacggtt cgcgaccctg 48760 gatgagttcc gtgcggccgt ggactcggac gttcctgccc cgggttcggt gttggtcgca 48820 gctatgtcgg ccgaagaggt cgagggtgga tccctgccgt cgcgcgccca agagtcgacc 48880 tccgatctgc tggctctcgt gcagtcgtgg cttgcggacg agcggttcgc cgaatcccag 48940 ctcgtggtcg tcacgcgtgc agcggtgtcg gccgactcgg attcggacgt cgcggacctg 49000 gtgggtgcgt cgtcgtgggg gttgttgagt tcagcccagt cggagaaccc gggtcgcttc 49060 gtgctggtgg acgtggacgg cacacctgag tcgtggcagg cgttgccggc cgccgtgcga 49120 gcaggagaac cgcagctggc acttcggcgc ggcgtggcgc tggtgcctcg gttggcgcga 49180 ctcacggtgc gcgaggaggg ctcctccccg caactcgaca cggacgggac cgtcctcatc 49240 acgggtggca ccggtgcgtt ggggggagtg gttgcccgtc acctggtgga ggagcacggg 49300 attcggcgtt tggtgttggc aggccggcgt ggctggaatg cgcctggagt ccacgagttg 49360 gtggatgagc tggcgcgcgc gggcgccgtg gttgaggtgg tggcttgcga tgtggctgac 49420 cgcaccgatc tggagcacgt gctggccgcc attccggtcg actggccgct gcgggggatc 49480 gtgcataccg ctggggtgct ggccgacgga gtgatcgggt ccttgtcggc ggcggatgtg 49540 ggcacggtgt ttgccccgaa ggtgacgggg gcatggcatc tgcacgagtt gacccgcgat 49600 ctggatctgt cgttcttcgt tcttttctct tccttctccg ggattgcggg tgccgcaggg 49660 caggccaact acgcggcggc gaacacgttc ctggatgcat tggcgcgtta tcgccgggcg 49720 cgtgggctgc ctgggttgtc gttggcgtgg ggactgtggg cgcaacccag cggtatgacg 49780 agtggcttgg acgcggcgtc ggtggagcgg ttggcgcgga cgggcatcgc agaactttcc 49840 acggaggatg gactccgcct gttcgatgcc gcgttcgcga aggaccgggc ttgcgtcgtt 49900 gccgctcgat tggacagggc gctgctggtc gggaacggac gatcgcacgc gattccggcg 49960 ctgttgagcg cgttggttcc tgttcgcggc ggtgtggcga ggaaaacagc caattctcag 50020 gccgcggatg aggacgcact gttgggtttg gtgcgggagc acgtttcggc cgtgctgggt 50080 tattcgggtg cggtcgaggt tgggggcgac cgtgctttcc gtgatctggg ttttgattcg 50140 ttgtctggcg tggagttgcg gaaccgcctt gccggggtgc tgggggtgcg gttgccggcg 50200 actgcggtgt tcgactatcc gacgccgcgg gcgctggcgc gtttcctgca tcaggaactg 50260 gcaggcgagg tcgcgtccac gtcgacgccg gtgaccaggg cagcgagtgc cgaagaggat 50320 cttgttgcga ttgtcgggat gggatgtcgt tttccgggtg gggtgtcgtc gccggaggag 50380 ctttggcggc tggtggccgg cggcgtggat gcggtggctg ggttcccaga cgatcgcggc 50440 tgggatctcg cggcgttgta cgatcctgat cccgatcgtc tcgggacctc gtatgtgtgt 50500 gagggcgggt ttctgcggga cgcggcggag ttcgatgctg acatgttcgg catcagcccg 50560 cgtgaggcgt tggcgatgga tccgcagcag cggttgctgc tggaggtcgc ctgggaaacc 50620 ttggagcggg ctgggatcga tccgttctcg ttgcacggca gccggaccgg tgtgttcgcg 50680 ggcttgatgt accacgacta tggggcccga ttcattacca gagcaccgga gggcttcgaa 50740 gggcacctcg ggacgggcaa tgcggggagc gtgctgtcgg gtcgggttgc gtattcgttt 50800 ggtttcgagg gtcctgcggt gacggtggat acggcgtgtt cgtcgtcgtt ggtggcgtta 50860 cacctggcgg gtcaagcact gcgggccggt gagtgcgaat tcgcccttgc cggtggcgtc 50920 acggtgatgt cgacgccgac gacgttcgtg gagttctccc gtcaacgggg tctggctccg 50980 gatgggcggt gcaagtcgtt cgcggcggcc gcggatggca ccgggtgggg cgagggtgcc 51040 ggtctggtgt tgctggagcg gttgtcggat gcccggcgca atgggcacga ggttctggcg 51100 gtggtgcggg gtagcgcggt gaaccaggac ggcgcgtcga atggcttgac tgcgccaaat 51160 ggtccgtcac agcaaagggt gatcacccag gcactcacga gtgccgggct gtccgtgtcc 51220 gacgtggatg ctgtggaggc gcatgggacg ggcacgcggc ttggtgatcc gatcgaggcg 51280 caggcgttga tcgctacgta cggccgggat cgtgatcccg gtcggccgtt gtggctgggg 51340 tcggtgaagt cgaatattgg tcacacccag gcggcggcgg gtgtcgctgg tgtgatcaag 51400 atggtgatgg cgatgcggca gggggagctg ccgcgcacgt tgcacgtgga cgagccctcc 51460 gcgcaggtgg actggtctgc gggcacggtc caactcctca cggagaacac gccctggccc 51520 gacagcggtc gtcttcgccg ggcgggcgtg tcatcgttcg ggatcagtgg caccaacgcg 51580 cacctgatcc ttgaacaacc tccgcgagag tcgcagcgct caacagagcc ggattcgggt 51640 tctgtccgcg attttccggt ggtgccgtgg atggtgtcgg gcaaaacacc cgaagcgcta 51700 tccgcccagg cagatgcatt gatgtcctac ttgagcaatc gcgttgatgc ttccccgcga 51760 gatatcggtt attcgcttgc ggtgacccgt ccggcgttgg accaccgcgc tgtcgtgctg 51820 ggtgcggatc gtgccgcgtt gctgccgggc ttgaaagcgc tggccgttag taatgacgct 51880 gccgaggtga tcaccggcac tcgtgccgct gggccggtcg gattcgtgtt ctccggtcaa 51940 ggtggtcagt ggcccgggat gggaagcggg ctccactcgg cgtttccggt gttcgccgac 52000 gcgtttgacg aagcctgctg cgagctggat gcgcatctcg ggcagatggc ccggctacga 52060 gatgtgttgt ccggttcgga tacgcaactt ctggaccaga ccttgtgggc gcagccgggc 52120 ctgttcgcgt tgcaagtcgg actctgggag ttgttgggtt cgtggggtgt ccggcccgct 52180 gtggtgctgg gccactcggt cggtgagctg gcggcggcgt tcgcggctgg agtgttgtcg 52240 ttgcgggatg cggctcggct ggtggcgggc cgtgcccggt tgatgcaagc cctgccaact 52300 ggcggtgcca tgctcgctgc ggctgctgga gaggagcagc tgcgcccgtt gctggccgac 52360 tgcggtgatc gtgtggggat cgccgcggtc aacgctcccg ggtcggtggt gctctccggt 52420 gatcgggatg tgctcgatga cattgccggt cggctggacg ggcaagggat ccggtccagg 52480 tggttgcggg tttcgcatgc gtttcattcg catcggatgg atccgatgct ggcggagttc 52540 accgaaatcg cccggagcgt ggactaccgg tcgtcagggc tgccgatcgt gtcgacgttg 52600 acgggtgagc tcgatgaggt cggcatgccg gctacgccgg agtattgggt gcgccaggtg 52660 cgagaacccg tccgcttcgc cgacggtgtt gctgcgctcg cggctcacgg tgtgagcacc 52720 gtcgtcgagg tcggtccgga tggggtgttg tcggcgctgg tgcaggagtg cgcggccgga 52780 tccgatcagg gcggacgggt ggccgcggtt ccgctcatgc gcagcaatcg cgacgaggcg 52840 cacacggtga caacggcatt ggcgcagatc catgtgcgtg gtgctgaggt ggactggcgg 52900 tcgtttttcg ccggtaccgg ggcaaagcag gtcgagctgc ccacgtatgc cttccaacga 52960 cagcggtact ggcttgactc accatccgaa ccggtcgggc aatccgccga tcccgcgcgc 53020 cagtcgggct tctgggaact cgtcgagcag gaagatgtca gcgcgctcag cgccgctctg 53080 cacattaccg gcgatcacga cgtgcaggcg tccctggaat cggtggttcc ggtcctctcc 53140 tcctggcatc gccggatccg caacgaatcc ctggtgcacc agtggcggta ccggatttcc 53200 tggcatgagc gggcagattt gccagacccc tcgttgtcgg ggacatggct cgtcgtcgtg 53260 ccggaggggt ggtcggcgag tcggcaagtt ctgcgtttca acgagatgtt cgaggaacgg 53320 ggttgcccgg cagttctgtt cgagctcgcc gggcacgacg aggaagccct ggcgcaacga 53380 ttccgctcgt tgcctgttgc gtcaggggga ataagcggcg tgttgtcctt gctggcgctg 53440 gatgaatcgc cgtcctcgcc gaacgctgct ttgccgaatg gcgcgctgaa ctcgttggta 53500 ctgctgcgag ctctgcgggc cgcggatgtg tcggcgccat tgtggttggc gacgtgtggt 53560 ggtgtcgcgg tcggggatgt gccggtgaac ccggggcagg cgctggtgtg gggactgggt 53620 cgcgtcgtcg gtctggagca tccggcctgg tggggtggcc tggtcgacgt gccgtgcttg 53680 ctcgatgagg acgctcgaga acgcttgtcg gtcgtgttgg caggtcttgg cgaggacgag 53740 atcgcggtac gtcccggtgg tgtgttcgtg cggcggttgg aacgcgctgg tgcggcgtcg 53800 ggtgccgggt cggtgtggcg tcctcggggg acggtgttgg tgacgggtgg tacgggcggt 53860 ttgggggcgc atgttgcccg gtggttggcg ggtgccgggg ctgagcatgt ggtgttgacc 53920 agccgtcgag gcgcggcggc tccgggcgct ggagatttgc gggcggagct ggaggcgctg 53980 ggcgctcggg tttcgatcac ggcctgcgac gtggccgatc gtgacgcttt ggccgaagtg 54040 ttggcgacca ttccggatga ttgcccgctg accgcggtga tgcatgcggc gggggtcgtt 54100 gaagtcggcg acgtggcgtc gatgtgtttg accgacttcg ttggggtgct gtcggcgaag 54160 gcaggtggtg cggcgaatct cgatgagttg ctcgccgatg tcgagctgga tgccttcgtg 54220 ctgttctcat ccgtctcggg tgtgtggggt gctggcgggc agggcgctta tgcggcggcg 54280 aatgcctact tggatgcgtt ggcgcagcag cgtcgggcaa gggggttggt ggggactgcg 54340 gttgcgtggg gcccgtgggc cggtgacgga atggccgcag gtgaaggcgg tgcacagctg 54400 cgccgggccg gcctggtgcc aatggctgcg gatcgggcgt tgctggcact tcagggcgca 54460 ttggatcgtg acgagacatc cctggtcgtg gccgatatgg cgtgggagag gttcgccccg 54520 gtgttcgcca tgtcccgtcg gcgtccgctg ctcgacgagc tgcccgaagc acagcaggcg 54580 ttggcggatg cggagaacac cactgatgct gcggactcgg ccgtcccgct accgcggctc 54640 gcgggcatgg cagccgccga acgccgccgc gcgatgctgg acctggtgct ggcggaggcc 54700 tcgattgtgt tgggacacaa cgggtctgac ccagttggtc ccgaccgggc gttccaggag 54760 ctcggatttg attcgctgat ggccgtcgaa ctgcgcaaca ggttgggcga ggcaacagga 54820 ttgagtctgc cggccacgtt gatcttcgat tatccgagcc catccgcgct ggctgagcag 54880 ctggtcggcg agctggtggg agcgcagccc gcgaccaccg tcgtggccgg ggccgatcca 54940 gtggatgatc cggttgtcgt ggtcgcgatg ggatgccggt atccgggcga cgtctgctcg 55000 cccgaggagc tgtggcagct ggtttctgcg ggacgtgatg cggtatcgac gttccccgtc 55060 gatcggggtt gggactgcaa cacgttgttc gacccggatc cggatcgggc aggcagtacc 55120 tatgtgcgag aaggtgcctt cctgaccggt gctgatcggt tcgacgccgg gttcttcggc 55180 atcagccctc gcgaggcgcg cgcaatggat ccgcagcaga ggttgttgct cgaagtggcg 55240 tgggaggttt tcgaacgagc aggaatcgct ccgctgtcgt tgcggggtag caggaccggt 55300 gtgttcgcgg ggaccaatgg gcaggaccac ggtgcgaaag tggctgccgc gccggaggcg 55360 gcgggtcacc tcctgaccgg aaacgccgcg agtgtcctgg ccggccggct ttcctacacg 55420 ttcggccttg aggggcctgc ggtggcggtg gataccgcgt gttcgtcgtc gttggtggcg 55480 ttgcatttgg cgtgccagtc gctgcgttcg ggtgagtgtg atatggcgtt ggcaggtggt 55540 gtgacggtga tgtcgacacc cctggctttc ctcgagttct ctcgtcagcg cggtttggcg 55600 ccagatggtc ggtgcaagtc gtttgcggcc gctgcggatg gcaccgggtg gggtgagggt 55660 gccggcctgg tgttgctgga gcggttgtcg gatgctcgtc ggaatggtca ccgggtgttg 55720 gccgtggttc gcgggtctgc ggtgaatcag gatggtgcgt cgaatggcct gactgcgccg 55780 aatggtccgt cgcagcagcg ggtgattcgg caggccctcg cgaatgcggg gctgtcggcg 55840 tccgatgtgg atgtcgtgga ggcgcacggg accggtaccg ggctcgggga tccgatcgag 55900 gcgcaggcgc tgatcgcgac atatgggcag gagcgggatc ctgagcgggc cctgtggctg 55960 gggtcgatca agtccaacat cggccacacg caggcggcgg ccggtgtggc gggggtcatc 56020 aagatggtgc aggccatgcg gcacggggag ttgcctgcga cgttgcacgt ggacaagccc 56080 actccacagg tggactggtc tgccggggcc gttcggctcc tcaccgggaa cacgccctgg 56140 cccgagagcg gccgtcctcg tcgagcgggg gtgtcgtcgt tcgggatcag cggcaccaac 56200 gcacacctca tcctcgaaca accaccgtcg gaaccagcgg agatcgacca atcggatcgg 56260 cgggtcactg cgcatccagc ggtgatcccg tggatgttgt cggctaggag tctcgcagcg 56320 ctgcaggccc aagcggctgc gctgcaggcc cggctggacc ggggtcctgg cgcttctccg 56380 ctggatttgg ggtattcact cgcgaccact cgttctgtgc tggacgaacg cgccgtcgtg 56440 tggggtgccg atcgggaggc actgctgtcc aggctggcag cgctcgccga tggccggacg 56500 gcgccggggg tgataacggg ctctgcgaat tccggtggcc gcatcggatt cgttttttcc 56560 ggtcagggca gtcagtggct ggggatggga aaggcgttgt gcgcggcttt cccggcgttc 56620 gcggacgcct tcgaggaagc ctgcgacgcg ctaagcgcac acctgggcgc ggacgttcgg 56680 ggtgtgctgt tcggtgctga tgagcagatg ctcgaccgga cgctgtgggc gcagtcgggg 56740 atcttcgcgg ttcaagtcgg cctcctggga ttgctgaggt cgtggggcgt gcggccggcc 56800 gcggtgctgg ggcactcggt cggcgagttg gctgcggcgc acgcggctgg tgtgttgtcc 56860 ttgccggacg ctgcacggtt ggttgcggct cgggcccacc tgatgcaggc attgcccacc 56920 ggcggcgcaa tgctcgcggt cgccaccagc gaggcggcgg tcggaccgct gctttccggg 56980 gtgtgcgatc gggtcagcat cgctgcgatc aacggccccg agtcggtagt gctctccggc 57040 gaccgcgatg tgctcgtgga gctcgcaggc gaattcgatg cccgagggct taggaccaaa 57100 tggttgcggg tctcccatgc tttccactcg caccggatgg aaccgattct ggacgagtac 57160 gcggaaaccg ccaggtgcgt cgagttcggt gaaccggtgg tgccgatcgt ctccgccgcg 57220 accggtgcgc tggacaccac cggactgatg tgcgcggccg actactggac gcgccaagtg 57280 cgtgatcctg tccgcttcgg agacggtgtc cgggcgctcg tcggccaagg cgtggacacg 57340 atcgtcgagt tcggcccgga cggggcgttg tcggccctgg tcgagcagtg cttggccggg 57400 tccgaccagg ctgggagggt ggcggcgatc ccgctgatgc gcagggaccg cgatgaggtc 57460 gagaccgcgg tggcggccct ggcgcacgtg cacgtccgcg gtggtgcggt ggactggtcg 57520 gcttgcttcg ccggcaccgg cgcccgcacc gtcgagttgc ccacctacgc cttccaacgc 57580 cagcggtact ggctggccgg gcaagcggac gggcgcggcg gcgatgtggt tgccgacccg 57640 gtcgacgcgc gcttctggga gttggtcgag cgcgccgatc cggaaccgtt ggtggatgaa 57700 ctctgcatcg accgggacca gcccttccgg gaggtgctgc ccgttctggc ttcctggcgc 57760 gagaaacaac gccaggaggc cctcgcggat tcctggcgct accaggtgcg ctggaggtcc 57820 gtcgaggtgc cgtccgcagc cgccctccgg ggcgtgtggc tggtggtgct tccagctgac 57880 gtgccccgag atcaaccggc ggtcgtcatc gacgcgctga tcgcgcgcgg cgccgaggtc 57940 gcggtcctgg aattgaccga gcaggacctc caacgcagtg cgcttgtgga caaggtgcgc 58000 gccgtcattg cggaccgcac cgaggtgacg ggtgtgttgt ctctgttggc gatggacggc 58060 atgccctgcg cggcgcatcc gcacctgtcc cgtggtgtcg ccgctaccgt gatcctgacg 58120 caggtgttgg gcgatgcggg tgtttccgcc ccgctgtggc tggccacgac cggtggcgtc 58180 gaggccggga ccgaggacgg tccggccgat ccggaccacg gcttgatctg ggggctcggc 58240 agggtcgtcg gccttgaaca tccgcagtgg tggggtggcc tgatcgacct tccggagaca 58300 ctggacgaga cgtcccggaa cgggttggtg gccgcactcg ccgggacggc ggccgaagat 58360 cagctcgccg tgcgttcatc cgggttgttc gttcgcagag tggtgcgcgc agcgcggaac 58420 ccccggtcag agacatggcg tagccgggga acggtcctca tcacgggcgg aacaggcgcg 58480 ctcggtgccg aggtcgcacg atggctggcc cggcggggag ctgagcacct ggtgttgatc 58540 agtcgccgcg gcccggaagc tcccggcgca gcggacctag gggccgagct gactgaactc 58600 ggcgtgaaag tcacagtctt ggcctgcgat gtgacggacc gcgacgagct ggcggcggtg 58660 ctggcggccg ttcccacgga gtatccgctg tcggcggtcg tgcacaccgc cggcgtcggg 58720 acgcctgcga acctggccga gacgaccttg gcgcagttcg ccgacgtgtt gtcggccaag 58780 gtcgtcggcg cggcgaacct ggaccggctg cttggcgggc aaccgttgga cgccttcgtg 58840 ctgttctcct cgatctcggg agtttgggga gccggcggcc aaggagccta ttcggccgcc 58900 aatgcgtatc tcgatgccct tgccgagcgc cgacgggctt gcgggcggcc ggcgacgtgc 58960 atcgcctggg gtccgtgggc gggtgcgggc atggccgttc aggaaggtaa cgaggcgcat 59020 ctccgccgaa ggggcctggt accgatggaa ccgcagtcgg ccctcttcgc gctgcaacag 59080 gccctgtccc aacgagaaac cgccatcacc gtcgcagatg tggactggga gcgattcgcc 59140 gcctctttca ccgcggcccg cccgcgacca ctgttggaag agatcgtgga tctacggccc 59200 gacaccgaga ccgaggagaa gcacggtgcc ggcgagctgg ggcagcagct ggccgcactg 59260 ccgcccgctg agcgcggaca cctgctgctg gaggtggtgc tggcggaaac cgccagcacc 59320 ctggggcacg attcggcgga ggctgtgcaa cccgatcgga ccttcgccga actgggcttc 59380 gattcgctga ccgcggtaga gctgcgcaac aggttgaacg cggtgaccgg gcttcgcctg 59440 ccgccgacgc tggttttcga ccacccgacg ccgctggcgt tgtccgaaca gttggttccg 59500 gccctggtcg cggagccgga caacggcatc gaatcgctgc tcgccgagct cgacaggctg 59560 gataccacgt tggcgcaagg gccttcgatc ccactggaag accaggccaa ggtggcggag 59620 cgcttgcacg cactcctcgc caagtgggac ggggcgcgtg acggcacggc cagagcgacg 59680 tcaccccaat cgctgacggc ggccacggac gacgaaatct tcgacctcat cgaccggaag 59740 ttccggcgct gaccgccctt tcctcgcctc agctcccctg attactggaa cggtgtattt 59800 cgatggccaa tgaagaaaag ctccgcgagt acctcaagcg tgtcgtcgtc gaactggaag 59860 aggcgcacga acgcctgcac gagttggagc gccaggagca cgaccccatc gcgatcgtgt 59920 cgatgggatg tcgttatccc ggtggcgtct ccactccgga ggagctgtgg cgactggtcg 59980 tcgacggagg agacgcgatc gcgaacttcc ccgaagaccg tggctggaat ctggacgagc 60040 tgttcgatcc tgatccgggc cgagccggga cctcctacgt ccgcgagggt ggtttcctgc 60100 gcggggtcgc ggacttcgat gccgggctct tcgggatcag tccgcgcgag gcacaggcga 60160 tggacccgca acagcggttg ctgctggaga tctcgtggga ggtgttcgag cgcgccggca 60220 ttgacccgtt ttctttgcgg ggtaccaaga ccggtgtgtt cgcgggcctg atctaccacg 60280 actacgcgtc gcggtttcgc aagacccccg cggagttcga gggttacttc gccaccggca 60340 acgcgggcag cgtcgcatcc ggccgggtgg cttacacctt cgggttagag ggcccggcgg 60400 tcaccgtgga caccgcctgc tcgtcgtccc tggtggcgct gcacctggcc tgccagtccc 60460 tgcggctggg cgaatgcgac ctggccctgg ccggtggcat ttcggtgatg gccacgccgg 60520 gagccttcgt cgagttcagc cggcaacgcg cactcgcctc ggatggccgg tgcaagccct 60580 tcgcggatgc cgccgacggc accggctggg gcgagggcgc cggaatgctg ctgctggaac 60640 ggctgtcgga cgcacgacga aacggccacc cggtgctggc ggcggtggtc ggttccgcga 60700 tcaaccagga cgggacgtcc aacggcctga ccgcgcccag cggtcccgca cagcagcgag 60760 tgatccgcca agccctggcg aacgccgggt tgtcgcccgc cgaggtcgat gtggtcgagg 60820 cgcacggcac gggcacggcc ttgggcgacc cgatcgaggc gcaggccctg atcgccacct 60880 acggggcgaa ccggtcggcg gatcatccgc tgctgctggg ttccctcaag tcgaacatcg 60940 gccacaccca ggctgccgcc ggtgtggccg gggtgatcaa gtcggtcctg gccatcaggc 61000 accgggagat gccccgcagc ctgcacatcg accagccatc gcagcacgtg gactggtcgg 61060 cgggcgcggt gcggctgctc acggacagcg ttgactggcc ggatctcggc aggccgcgcc 61120 gagcaggggt gtcctcgttc ggcatgagcg gtaccaacgc acacctgatc gtcgaggaag 61180 tatccgacga gccggtctcg ggcagtaccg agccgaccgg ggcatttccc tggccgctgt 61240 ccggcaagac ggagacggca ttgcgcgagc aggctgccga gttgctctcc gtagtgaccg 61300 agcacccgga gccgggactg ggggacgtcg ggtactcgct ggccaccggt cgcgctgcga 61360 tggagcaccg ggctgtcgtg gttgccgacg atcgggactc tttcgtcgcc ggactgacgg 61420 cgttggctgc gggcgttccg gcagccaacg tggtgcaggg cgcggccgac tgcaagggaa 61480 aggtcgcgtt cgtgttcccc ggccagggct cgcattggca ggggatggcg agggaactgt 61540 ccgaatcctc gccggtgttc cggcggaagc tggcggaatg cgcggcggct acggcccctt 61600 acgtggactg gtcgctgctc ggcgtccttc gcggtgatcc cgatgcaccc gcgctggatc 61660 gcgacgacgt gattcagctc gcgctgttcg ccatgatggt gtcgctggcc gaactgtggc 61720 gttcgtgcgg agtggagccc gccgcggtgg tcggtcattc ccagggcgag atcgccgccg 61780 cccatgtggc aggcgctttg tccttgactg atgcggtgcg catcatcgct gcccgctgcg 61840 atgcggtgtc ggcgctgacc gggaagggag gcatgctcgc gattgccttg ccggaaagcg 61900 cggtggtgaa gcgaatcgca ggcctgccgg agctgaccgt tgcggcggtc aacggacccg 61960 gctccactgt cgtttccggc gaaccgtcgg ctctggagcg tctgcagacc gaactgaccg 62020 cggaaaacgt gcagacccgg cgggtgggaa ttgattacgc ctcgcattcg ccgcagatcg 62080 cgcaggtcca gggccggctt ctggaccggc tgggcgaagt cgggtccgaa cctgctgaga 62140 tcgctttcta ctcgacggtc accggcgagc ggacggacac cggccgactc gacgccgact 62200 actggtacca gaaccttcgg cagcccgtcc gcttccagca gaccgtcgcc cggatggcag 62260 atcagggcta tcggttcttc gtcgaggtga gcccgcaccc gctgctcacc gccggaatcc 62320 aggaaacgct ggaagccgcg gacgcgggcg gggtggtggt cggttcgctg cggcgtggcg 62380 agggcggctc ccggcgctgg ctgacttcgc tggccgagtg ccaggtgcgc ggactgccgg 62440 tgaattggga acaggtattc ctcaacaccg gagcccgacg cgtgccgctg ccgacctacc 62500 cgttccagcg gcagcggtac tggttggagt ccgccgagta cgacgcgggc gatctcggtt 62560 cggtgggctt gctctccgcc gagcatcccc tgctcggggc tgcggtgacg ctggccgatg 62620 cgggcgggtt cctgctgacc ggcaagctgt cggtcaagac ccagccctgg ttggccgacc 62680 acgtggtcgg cggggcgatc ctgctgcccg gcaccgcgtt cgtggaaatg ctgatacgcg 62740 ccgcggacca ggtcgggtgc gatctgatcg aggagttgtc cctgacgact ccgctggttt 62800 tgcccgcgac cggtgcggtg caggtgcaga tcgcggttgg cggtccggac gaggccgggc 62860 gccgctcggt ccgcgtgcat tcctgtcgag acgacgccgt gccgcaggac tcgtggacct 62920 gccacgcgac cggcacgttg acctccagcg atcaccagga cgccggccag ggccccgatg 62980 ggatttggcc gcccaacgat gctgtcgcgg ttccgctgga cagcttctac gcccgcgcag 63040 ctgagcgggg cttcgatttc ggcccggcgt tccaggggtt gcaggcggct tggaagcgcg 63100 gagacgagat cttcgccgag gtcggcctgc ccaccgcaca ccgcgaagac gccggcaggt 63160 tcggaatcca ccctgctctg ctggatgcgg cactgcaggc gctgggcgca gccgaagagg 63220 atccggacga gggatggctc ccgttcgcgt ggcaaggtgt gtccctcaaa gcgacgggcg 63280 cactttccct tcgggtgcac ctcgttccgg cgggcgcgaa tgcggtgtcg gtgttcacga 63340 ccgacacgac tggccaagcc gtgctctcca tcgattcgct ggtgctgcgc cagatttcgg 63400 acaagcagtt ggcagcggcc cgtgcgatgg aacacgagtc cctgttccgg gtcgactgga 63460 agcgaatctc gcccggcgct gccaagccgg tctcctgggc agtgatcggc aatgacgaac 63520 tcgcccgagc ctgcggctcg gcacttggca cggaactcca ccccgacctg accgggttgg 63580 ctgacccgcc cccggacgtc gtggtggtgc catgcggtgc gtctcgccag gacttggacg 63640 ttgcttccga ggcacgtgcc gcgacacaac gcatgcttga cctgatccag gattggttgg 63700 cggcggcgcg attcgccgga tctcgcctgg tggttgtgac gtgtggtgcg gcgtcgacag 63760 gtcccgccga gggtgtttcc gacctggtgc atgctgcgtc gtggggtttg ttgcgttcgg 63820 cgcagtcgga gaacccggac cgattcgtgt tggtcgatgt ggacggaacc gccgaatcat 63880 ggcgtgcgct cgcggcggcc gtgcgttccg gagaaccgca gctggcgttg cgcgccggtg 63940 aagtccgggt gcctcgcctg gcgcgatgtg ttgccgccga ggacagccgg atcccagtgc 64000 ccggtgcgga tgggacggtg ttgatttccg gcggtacggg cctgctgggc gggttggttg 64060 cccggcattt ggtggcggag cgcggtgtcc gccgcctggt gctcgcgggg cgacgcggct 64120 ggagcgcccc cggggtcacc gacctggtgg atgagttggt gggcctggga gctgcggtcg 64180 aggtggcgag ctgcgatgtc ggggatcggg cccagttgga ccggctgctg acgacgatct 64240 cggcagagtt cccgctgcgc ggagtggtgc atgcggccgg ggcacttgcc gacggggtcg 64300 tcgagtcgct gacaccagag cacgtggcaa aggtgttcgg cccgaaggcc gccggtgcgt 64360 ggcacctgca cgagttgact cttgatctgg atctctcgtt cttcgtgctc ttctcctcgt 64420 tctccggcgt ggcgggggct gcgggtcagg gaaactacgc ggcggcgaac gcgttcctgg 64480 acggcctggc tcagcaccgg cggacggcgg ggctgcctgc ggtgtcgctg gcttggggct 64540 tgtgggagca gcccagcggg atgaccggag cgctcgatgc ggcgggccgt agccgcattg 64600 cgcgcaccaa tccgccgatg tccgcgccgg acgggttgcg gctgttcgag atggcgtttc 64660 gcgttccggg cgaatcgctt ctggttccgg tccacgtcga cctgaacgcc ctgcgcgctg 64720 atgcggccga cggcggtgtg cctgcgttgt tgcgcgacct ggtgccagcg cccgtgcggc 64780 ggagcgcggt caacgagtcg gcggacgtca acggtctggt tggtcggctg cggaggctgc 64840 cggacctgga tcaggaaacc cagctgttgg gtttggtgcg cgagcatgtt tcggcggtgc 64900 tggggcattc gggtgcggtc gaggtcgggg ccgatcgtgc tttccgggat ttgggttttg 64960 attcgttgtc cggtgtggag tttcggaacc ggcttggcgg ggtgctgggc gttcggttgc 65020 cggctactgc ggtgttcgac tatccgacac cgcgggcgtt ggttcggttc ttgctcgaca 65080 aactgattgg tggcgtggag gctccgactc ccgcaccggc ggctgtggcg gcggtgactg 65140 ctgacgatcc cgttgtgatc gtggggatgg gctgtcgtta tccgggtggg gtgtcctcgc 65200 cggaggagct ttggcgtttg gtggccgggg gcttggatgc ggtggcggag ttcccggacg 65260 atcgtggctg ggatcaggcg gggttgttcg atccggatcc cgatcgtctt gggacctcgt 65320 atgtgtgtga gggtggcttc ctgcgagatg cggcagagtt cgatgccggt ttcttcggga 65380 tttccccgcg tgaggcgttg gcgatggatc cgcagcagcg gttgctgctg gaagtcgctt 65440 gggaaaccgt ggagcgggcg gggattgatc cgctttcgtt gcgggggagc cggaccggcg 65500 tgttcgcggg gctgatgcac cacgactacg gcgcgcggtt catcacgagg gcgccggagg 65560 gtttcgaggg ttatctaggt aatggcagcg cgggaggcgt gttttcgggt cgggttgcgt 65620 attcgtttgg tttcgagggt cctgcggtga cggtggatac ggcgtgttcg tcgtcgttgg 65680 tggcgctgca cctggcgggt caagcactgc ggtctggtga gtgtgatctg gctcttgcgg 65740 gtggtgtgac ggtgatggcc acgccgggga tgttcgtgga gttttcgcgt caacggggct 65800 tggcggcgga tgggcggtgc aagtcgtttg cggcggctgc ggatggcacc ggttggggag 65860 aaggcgcggg cttggtgttg ttggagcggc tgtcggatgc ccggcgcaac gggcacgcgg 65920 ttctggcggt cgtgcggggt agcgcggtga atcaggatgg tgcgtcgaat ggtttgacgg 65980 cgccgaatgg gccctcgcag cagcgggtga tcacgcaggc gttggcgagt gctggtttgt 66040 cggtgtctga tgtggacgcc gtggaggcgc atgggactgg aaccaggctt ggtgatccga 66100 ttgaggcgca ggctctgatt gccacttacg ggcaggggcg ggatagcgat cggccgttgt 66160 ggttggggtc ggtgaagtcg aatattggtc atacgcaggc ggcggcgggt gtcgctggtg 66220 tgatcaagat ggtgatggcg atgcggcacg ggcagctgcc cgcgacgttg catgtggatg 66280 aacctacgtc ggaagtggat tggtcggcgg gggatgtcca gctcctcacg gagaacaccc 66340 cctggcccgg caacagccat cctcggcggg tgggcgtgtc gtcgttcggg atcagcggca 66400 ccaacgcaca cgtcatcctc gaacaagcct cgaaaacacc agacgagact gcggacaaga 66460 gcggtcccga ttcggaatcg accgtggacc ttccagcggt cccgttgatc gtgtcgggga 66520 gaacaccggc agcgctcagc gctcaggcga gcgcattgtt gtcctatttg ggtgagcgtg 66580 gcgatatttc cacgctggat gcggcgtttt cgttggcttc ctcccgggcc gcgttggagg 66640 agcgggcggt ggtgctggga gcggaccgcg aaacgttgtt gtccgggttg gaagcgctgg 66700 cttccggtcg cgaggcttct ggggtggtgt cgggatcccc ggtctctggc ggggttgggt 66760 tcgtgttcgc cggtcagggc ggacagtggt tggggatggg ccgggggctc tactcggttt 66820 ttccggtgtt cgctgacgcg tttgacgaag catgtgccgg actggacgcg catctggggc 66880 aggacgtggg ggtccgggat gtggtgtttg gttccgacgg gtccttgttg gatcggacgc 66940 tgtgggccca gtcgggtttg ttcgcgttgc aggttggttt gctgagcctg ctgggttcgt 67000 ggggtgtccg gccgggtgtg gtgctgggcc attcggtcgg cgagttcgcg gcggcggttg 67060 cggcgggagt gttgtcgttg ccggatgcgg ctcggatggt ggcgggtcgt gcccggttga 67120 tgcaggcgtt gccttctggc ggtgccatgt tggcggtggc tgctggtgag gagcagctgc 67180 ggccgttgtt ggccgatcgg gttgatggtg cgggtatcgc cgcggtcaac gctcctgagt 67240 cggtggtgct ctccggcgat cgggaggtgc ttgacgacat cgccggcgcg ctggatgggc 67300 aagggattcg gtggcggcgg ttgcgggttt cgcatgcgtt tcattcgtat cggatggacc 67360 cgatgttgca ggagttcgcc gaaatcgcac gcagcgtgga ctaccggcgt ggcgacctac 67420 cggtcgtgtc gacgttgacg ggtgagctcg acaccgcagg tgtgatggct acgccggagt 67480 attgggtgcg tcaggttcga gagcccgtcc gcttcgccga cggcgtccgg gtgctcgcgc 67540 agcaaggggt cgccacgatc ttcgaactcg gccctgatgc gacgctgtcg gccctgattc 67600 ccgattgtca ttcgtgggct gatcaggcca tgccgattcc gatgctgcgt aaagaccgta 67660 cggaaaccga aactgtggtc gccgcggtgg cgcgggcgca cacgcgtggt gttccggtcg 67720 aatggtcggc gtatttcgcc ggcaccgggg cacggcgggt cgagttgccg acgtatgcct 67780 tccagcggca gcggtactgg ctggaaacat cggattacgg cgatgtgacg ggtatcggcc 67840 tggctgcggc ggagcatccg ttgctggggg ccgtggttgc gctggccgat ggtgatggga 67900 tggtgctgac cggccggttg tcggtgggga cgcatccgtg gctggcccag catcgcgtgc 67960 tgggcgaggt cgtcgtcccc ggcaccgcca tcctggagat ggccctgcac gcaggggcgc 68020 gtctcggctg tgaccgggtg gaagagctca ccctggaaac accgctggtg gtccccgaac 68080 gcgcggcggg tgccggtagt cgtggccctg cgggagggac cacagtttca attgaaactg 68140 cggaagaacg tgtgcggacg aacgacgcca tcgaaatcca gctgctggtg aacgcacccg 68200 acgaaggcgg tcggcgaagg gtgtcgctgt attcccgccc ggccggtggg tcgagaggtg 68260 ggggttggac gcgccacgcc accggcgaac tcgtcgtcgg caccaccggt ggtagggcgg 68320 ttcctgattg gtcggctgag ggtgccgagt cgattgctct cgatgagttc tacgtcgctc 68380 tggccggaaa cgggttcgag tacgggccgt tgttccaggg gcttcaggcg gcatggcgtc 68440 gtggtgacga ggttctcgcc gaaatcgccc cgccggccga ggccgatgcg atggcgtcgg 68500 gatacctgct cgacccagcg ttgctggatg ccgcgctgca ggcgtccgcg ctcggcgacc 68560 gcccggagca aggcggcgcg tggctgccgt tctcattcac cggcgtcgaa ctttccgctc 68620 cggcagggac gatcagcagg gtgcggctgg agaccaggcg acccgacgcg atatcggtgg 68680 ccgtgatgga tgagagtggg cggttgctcg cctcgatcga ttctctcagg ctacgaagcg 68740 tgtcgtcggg acagctggcg aatcgggacg ctgtccgcga cgcgctgttc gaggtgacct 68800 gggagccggt ggcgacgcag tcgacggaac cgggtcgctg ggccctgctt ggtgatactg 68860 cctgcggtaa agacgatctc atcaaactcg caacggattc cgccgaccgc tgcgcggatc 68920 tggcggcgct agccgagaaa cttgattcca gcgcgctggt tcctgatgtc gtggtctact 68980 gcgccggaga acaggcggat cccggcaccg gcgcagccgc acttgcggag acccagcaga 69040 cgttggctct gctccaagcg tggttggctg agccgcggtt ggccgaggca cgtctggtgg 69100 tggtgacgtg tgcagcggtg acgacggctc cgagtgacgg tgcatcagag ctggcacatg 69160 cgccgttgtg ggggttgttg cgtgccgcgc aggtggagaa cccggggcag tttgtgctgg 69220 cggacgtcga cggaaccgcc gaatcgtggc gtgcgttgcc gagtgcgttg ggctcgatgg 69280 aaccgcagtt ggccctgcgg aagggcgcgg tgcgagcgcc ccgcttggct tcggtcgccg 69340 ggcagatcga cgtgcccgcg gttgtggcgg atcccgaccg aaccgtgctg atttcgggcg 69400 gcacgggcct gttggggggc gcggttgccc gccacctggt gaccgaacgc ggtgtccgcc 69460 gattggtgtt gacgggccgt cgtggctggg atgctcctgg aatcaccgag ttggtgggtg 69520 agctgaacgg cctcggtgcc gtggtcgacg tggtggcgtg cgacgtcgcg gatcgtgctg 69580 atctggagtc gttgctggcg gcggtcccgg cggaatttcc gttgtgcggc gtggtgcatg 69640 ccgcgggggc gctggccgac ggggtgatcg agtcgttgtc accggacgac gtgggagcgg 69700 tgttcggccc gaaggcggcg ggggcgtgga atctgcacga gctgactcgt gatacggacc 69760 tgtcgttctt cgcgttgttc tcctcgcttt ccggtgttgc cggcgctcct ggtcagggca 69820 attatgcggc ggcgaacgcg ttcctggacg cattggcgca ttaccggcgg tcacagggac 69880 tgcctgcggt gtcgctggcc tggggcctgt gggagcagcc gagcgggatg acggagacgc 69940 tcagcgaggt cgaccggagc aggatcgcgc gcgccaaccc gccgttgtcc accaaggagg 70000 gattgcggct gttcgatgcc gggctggcgc tggaccgggc agcggtagtt ccggcgaagt 70060 tggacaggac tttcctggcc gagcaggcgc ggtcgggctc gctgcccgca ttgttgacgg 70120 cactggtacc ccccatccgt cgtaataggc gggctagcgg aaccgagctc gcggacgagg 70180 gcaccctgct cggggtggtg cgggagcatg ccgcggccgt gctggggtat tcgagcgcgg 70240 ctgacgtcgg ggtcgagcgc gctttccggg atctgggttt tgattcgttg tctggtgtgg 70300 agttgcggaa ccgccttgcc ggggtgctgg gggtgcggtt gccggcgact gcggtgttcg 70360 actatccgac gccgagggcg ctggcccggt tcctgcacca ggaactggca gacgagatcg 70420 ctacgacgcc agcgccggtg acgacgacca gggcaccggt cgccgaagac gatctcgtcg 70480 cgatagtcgg gatgggatgc cgttttcccg gtcaggtgtc ctcgccggag gagctctggc 70540 gtttggtggc cgggggcgtg gatgcggtcg cggacttccc agccgatcgc ggctgggatc 70600 tggcaggctt gttcgatccg gacccggaac gggctgggaa gacctacgtg cgggaagggg 70660 ccttcctcac cgacgccgat cggttcgatg cgggtttctt cgggatttcc ccgcgtgagg 70720 cgttggcgat ggatccgcag caacggctgt tgctggagct gtcctgggag gccattgaac 70780 gggcagggat cgatccgggt tcgctgaggg ggagtcggac cggtgtgttc gcggggctga 70840 tgtaccacga ctatggcgcc cggttcgcca gccgagcccc ggaaggtttc gaggggtatc 70900 tcggcaatgg cagtgctggg agtgtcgcgt cgggccggat tgcgtactcg tttggtttcg 70960 agggtcctgc ggtgacggtg gatactgcgt gttcgtcgtc gttggtggcg ttgcatttgg 71020 cgggtcagtc gttgcgttcc ggcgaatgcg atctcgccct tgccggtggt gtgacggtga 71080 tgtcgacgcc cgggacgttt gtggaattct cccgtcagcg gggcctggca ccggacgggc 71140 ggtgcaagtc gttcgcggag agcgcggacg gtaccggttg gggtgagggt gctggtttgg 71200 tgttgttgga gcggttgtcg gatgctcggc ggaatgggca tcgggtgttg gcggtggttc 71260 gtgggtcggc ggtgaatcag gatggtgcgt cgaatggctt gaccgcgccg aatggtccct 71320 cgcagcagcg ggtcatccag caggcgttgg cgagtgcggg tctgtcggtg tccgatgtgg 71380 atgccgtgga ggcgcatggg accgggacca ggttgggtga tccgattgag gcgcaggctc 71440 tgattgctac gtatgggcgc gatcgtgatc ccggtcggcc gttgtggttg gggtcggtga 71500 agtccaacat cggtcatacg caggcggcgg cgggtgttgc cggtgtgatc aagatggtga 71560 tggcgatgcg gcacgggcaa cttccgcgca cgctgcacgt ggatgcaccc tcctcgcagg 71620 tggattggtc ggcggggagg gtccagctcc tgacggagaa cacgccctgg cccgacagtg 71680 gtcgcccctg tcgggtgggg gtgtcgtcgt tcgggatcag cggcaccaac gcgcacgtca 71740 tcctggaaca gtccacgggg cagatggatc aggcagcgga gccggattcg agtcctgttc 71800 tggatgttcc ggtggtgccg tgggtggtgt cgggcaaaac acccgaagcg ctatccgccc 71860 aggcggcaac gttggcgacc tatttggacc aaaatgttga tgtctcccct ctggacgttg 71920 ggatttcgct tgcggtgacc cgttcggcgc tggatgagcg ggcggtggtg ctggggtcgg 71980 atcgtgacac gttgttgtct ggcctgaatg cgctggctgc cggtcatgag gctgctggcg 72040 tggttacggg acctgtcggg attggtggcc ggaccgggtt tgtgttcgcc ggtcaaggcg 72100 gtcagtggtt ggggatgggc cgccggttgt actcggagtt tccggcgttc gccggtgctt 72160 tcgacgaagc atgcgccgag ctcgatgcga acctggggag ggaagtcggg gttcgggatg 72220 tggtgttcgg ctccgacgag tccttgctgg atcggacttt gtgggcgcag tcgggtttgt 72280 tcgcgttgca ggtcggtctc tgggaattgt tgggtacgtg gggtgttcgg cccagcgtag 72340 tgctggggca ttcggtcggg gagctagccg cggcgttcgc cgcaggtgtg ctgtcgatgg 72400 cggaggcggc tcggctggtg gcgggtcgtg cgcggttgat gcaggcgttg ccttctggcg 72460 gtgccatgct ggcggtgtcc gcgaccgagg cccgagtcgg cccgctgctc gatggggtgc 72520 gggatcgtgt tggtgtcgca gcggttaacg ctccggggtc ggtggtgctt tccggtgacc 72580 gggatgtgct cgatggcatt gccggtcggc tggacgggca aggtatccgg tcgaggtggt 72640 tgcgggtttc gcacgcgttt cattcgcatc ggatggatcc gatgctggcg gagttcgccg 72700 agctcgcacg gagcgtggac taccggtctc cacggctgcc gattgtctcg acgctgaccg 72760 gaaacctcga tgacgtgggc gtgatggcta cgccggagta ttgggtgcgc caggtgcgag 72820 agcccgtccg cttcgccgac ggtgtccagg cgcttgtgga ccaaggcgtc gacacgattg 72880 tggaactcgg tccggacggg gcgttgtcga gcttggttca agagtgtgtg gcggagtccg 72940 ggcgggcgac ggggattccg ttggtgcgga gagaccgtga tgaggtccga acggtgctgg 73000 acgctttggc gcagacccac actcgtggtg gcgcggtgga ctgggggtca tttttcgctg 73060 gtacgagggc aacgcaagtc gaccttccca cgtatgcctt ccaacgacag cggtactggc 73120 tggagccatc ggattccggt gatgtgaccg gtgttggcct gaccggggcg gagcatccgc 73180 tgttgggtgc cgtggtgccg gtcgcgggcg gcgatgaggt gctgctgacc ggcaggctgt 73240 cggtggggac gcatccgtgg ctggcggaac accgcgtgct gggcgaagtc gtcgtccccg 73300 gcaccgcgtt gctggagatg gcgtggcggg ccggtagcca ggtcggttgt gaacgtgtgg 73360 aggagctcac cttggaggca ccgctggtcc tgccggagcg gggcgctgcg gcggtgcagt 73420 tggcggtggg ggctccggat gaggccggcc ggcgcagttt gcagctctat tcccgaggcg 73480 ctgatgaaga cggcgactgg cggcggattg cctccgggct gttggcccag gccaatgcgg 73540 tgccgccggc ggattcgacg gcatggccgc cggacggcgc cgggcaggtc gatctggcgg 73600 agttctacga gcgcctcgcc gagcgcggct tgacctacgg tccggtattc caagggctcc 73660 gcgccgcatg gcggcacggc gacgatatct tcgccgaatt ggccgggtca ccagacgcct 73720 cgggtttcgg catccacccg gcgctgctgg acgctgcact gcacgcgatg gcgcttggtg 73780 cttcgcccga ctcggaagcg cgtctgccgt tttcctggcg tggcgcccag ctgtaccgcg 73840 ctgaaggagc agcgcttcgg gtacggctct cgccgctggg ctccggtgca gtctcattga 73900 cgttggtgga tgccacaggg cgacgagtcg ctgcggtgga atcgctttcg acgcgaccgg 73960 tctccaccga ccagatcggt gccggtcgcg gcgatcaaga gcggctgctg cacgtcgagt 74020 gggtaaggtc ggctgaatct gcggggatgt ctctgacctc ctgcgcggtg gtcggtttgg 74080 gcgaaccgga gtggcacgct gcgctgaaga ccactggtgt ccaagtcgag tcccatgcgg 74140 accttgcttc gttggccacc gaggttgcca agcggggttc agctcctggt gcggtcatcg 74200 tcccgtgccc gcgaccccga gcgatgcagg agctgccgac cgccgcgcga agggcgacgc 74260 aacaggcgat ggcgatgctg cagcaatggc ttgccgatga ccggttcgtc agtacgcgcc 74320 tgatcctgct gacgcatcgg gcggtctccg cagttgctgg agaagacgtg ctcgacctgg 74380 tacacgcgcc gctgtggggc ttggtccgca gcgcgcaagc ggagcacccg gaccgattcg 74440 ccttgatcga tatggacgac gagcgagcat cgcagacggc actcgccgaa gcgctgactg 74500 cgggagaagc gcagctcgcg gtgcggtcgg gagttgtgct ggcgccccgc ctcggccagg 74560 tgaaggtgag tggaggtgaa gcgttcaggt gggatgaagg caccgtgctg gtcaccggcg 74620 gaaccggcgg gctcggggcc ctgctcgcac gccatctggt cagcgcccac ggtgtgcggc 74680 acctgttgct cgcaagtcgc cgtggtctgg cggcgcccgg agcggatgag ctggtggccg 74740 agctggagca ggccggcgcc gacgtcgcgg tcgtcgcgtg cgactcggca gatcgggact 74800 cgcttgcgcg gctggtggcg tcggtgcctg cggaaaaccc gttgcgggtg gtggtgcacg 74860 ccgccggtgt gctggatgac ggtgtgctga tgtcgatgtc gccggagcgc ttggacgcgg 74920 tgttgcggcc caaagtggat gccgcgtggt acctgcacga gctgactcgg gaactcggtc 74980 tgtcggcgtt cgtgttgttc tcctcggtcg cgggcctgtt cggcggtgcg gggcagagca 75040 attacgctgc cggcaacgct ttcctggatg ccttggcgca ttgccggcag gcccaggggc 75100 tgcccgcgct gtcgctggcc tccgggctgt gggcgagtat cgatggaatg gcgggcgacc 75160 tcgctgcggc agatgtggag cggctgtcgc gggcaggcat tggcccgctt tcggcaccgg 75220 gagggctggc cttgttcgac gctgccgttg gctcggacga accgttgctg gcaccggtgc 75280 gactggatgt cgaagcactg cgtgtgcagg cccgatccgt gcagacccgg attccggaaa 75340 tgctgcatgg catggcaatg gggccaagcc gccgcactcc gttcacttcc agggttgagc 75400 cgttgcacga acggctggcc ggattgtcgg agggcgaacg tcggcagcaa gtgctccagc 75460 gcgtccgcgc cgatatcgcg gtggtactgg ggcacggcag gtcgagcgat gtggacatcg 75520 agaagccttt ggccgagctg ggtttcgact cgctgacggc catcgaactc cgcaaccgtc 75580 tcgctaccgc caccggactg cggcttcccg cgacgctggc cttcgaccac ggcactgcgg 75640 cggcactcgc ccagcacgtg tgcgcgcagc taggcaccgc gaccgcgccg gcaccgaggc 75700 gaaccgacga caacgacgcc acggagcccg tgaggtcgct cttccaacag gcgtatgcgg 75760 ctggccggat acttgacggg atggatttgg tgaaggtcgc tgcccagttg cgaccggtgt 75820 tcggttcgcc tggcgagctg gaatccctgc cgaaacccgt ccagctttcc cgtggtcccg 75880 aagagcttgc cttggtgtgc atgccggcgc tgatcgggat gccgcccgca cagcagtacg 75940 cgcggatcgc cgccgggttc cgcgatgtgc gggacgtttc ggtgatcccg atgcctggat 76000 tcattgcggg agaaccgctg ccgtccgcca tcgaggtggc ggttcggacg caggcggagg 76060 cggtgctgca ggaattcgcc gggggctcgt tcgtactggt cgggcattcc tccgggggct 76120 ggctggcgca cgaggtagcc ggtgagctgg agcgtcgcgg ggtcgtcccg gccggggtcg 76180 tactgctgga cacctacatc cccggtgaga tcacgccgag gttctccgtg gcgatggccc 76240 accggacgta tgagaagctc gcgactttca cggacatgca ggatgtcggt atcaccgcga 76300 tgggcgggta cttccggatg ttcaccgagt ggactccgac gccgatcggt gctccgacgc 76360 tgttcgtgcg gaccgaagat tgcgtcgcag accctgaagg gcggccgtgg acagatgact 76420 cctggcggcc agggtggact ctcgcggatg ccacggtcca ggtgccgggc gaccacttct 76480 cgatgatgga cgagcacgcc gggtccaccg cacaggcagt cgcgagttgg cttgacaaac 76540 tcaaccagcg caccgctcgg caacgctgac gggcgtcctt ttaggacctt ctgggcggca 76600 ccggccaccc cggcggtgcc gccttccgtg gtccaggctc gccgatcttg acggcgcacg 76660 atgcgcggca cgcgcgctga tcgtgattcc gctgccgctc gtggccatcg gcctggcgaa 76720 tcatgtcctt tcgggcaacg tcaaacgaat tcgtccgagc ccgcattccg aggtgagggg 76780 cacccttggg tggctgagcc gctcaagggt gcccctcacc tcgaaattcg tccgatttgg 76840 gcggtggacg caaccccggt gggcgtggtg cgtctttctt gttgacagag cggtgagaag 76900 ccgctgacac acctgagagg aaaaggggag catgatgctc aagcgccacc gtttgacgac 76960 cgccatcacc ggccttctgg ggggagtact gctggtcagc ggctgcggaa ccgccgccgc 77020 acttcagtcc tcgccggcgc ccgggcatga cgcgcgcaat gttggtatgg cctcgggcgg 77080 gggcggcggg gacatcggca cgtcgaactg ctcggaggcc gatttcctcg ccaccgcgac 77140 accggtgaaa ggcgaccccg gcagtttcat cgtggcgtac gggaaccggt cggacaagac 77200 ctgcacgatc aacggcggcg tgccgaacct caagggcgtg gacatgagca actcgccgat 77260 cgaggacctg ccggtcgagg acgtgcggct tcccgacgcg cccaaggaat tcaccctcca 77320 gcccggtcag agcgcgtacg ccggcattgg catggtcctg gccgacagcg gcgacccgaa 77380 cgcccatgtc ctcaccgggt tccagtcctc gctgccggac atgtccgagg cccagccggt 77440 caacgttctc ggcgacggca acgtgaagtt cgccgcgaag tacctgcgag tcagctcgct 77500 ggtgtctacc gcagacgagc tgcgctaaaa cccatgtgag tcccgcagat tcgacctcgc 77560 cgtgcggcgc ctccggcgaa gcgtccgtac gtttgtcgtt gtgaccagcg ttgttcacgt 77620 ccgggcgcag cgctggtaca tactcaggcg tctcgggcgc ctccaacggg gcctggcatc 77680 cggggccgtc gagtgcggcg gcgctgacgc gttctctgtc gggcgttgtc acgccgccgg 77740 cctcgaaccg gtcccgcccc gtcggagccg gtggtccagc gcggtgtggc ggcggccgga 77800 gccgacggtg cgcaccgcct gcccgagggc ctttttcgaa ccgacgagga ccacgacctt 77860 cttggcccgg gtgaccgccg tgtagagcag gttgcgctgc agcatcatcc aggcgcttgt 77920 ggtcaagggg atcaccacgc acgggtattc gcttccctgc gaacgatgga tggtcaccgc 77980 gtaggcgtgg accagttcgt cgagttctgt gaagtcgtag tcgatgtcct cgtcctcgtc 78040 ggttcgcacg gtcatggtct gtgcttcgtt gtcgagggcg gacacgacgc cctgcgtgcc 78100 gttgaacacg ccgttggcgc ccttgtcgta gttgttgcgg atctgcgtga ccttgtcgcc 78160 gacgcggaag atccgtccgc cgaaccgccg ctctggcagg ccctccctgg ccggggtgat 78220 cgcttcctgc aacagctggt tcagcgcgcc tgcacctgcg gggcctcgat gcatcggggc 78280 gaggacctgc acgtcggtgc gcgggttgaa ccggaacttc cgcggaatcc ggcgggcgac 78340 gacgtcgacg gtgagctcgg cggtcggttc gctttcctct acgtggaaca ggaagaagtc 78400 ggtcagcccg tgtgtcagcg gatagtcccc ggcgttgatt cggtgcgcgt tggtcaccac 78460 cccggactcg gcggcctgcc ggaacacctc gttgagccgc acgtgtggaa tcggggtgcc 78520 aggggcgagc agatcgcgca gtacctcacc ggctccgacc gacgggagct ggtcgacgtc 78580 gccgaccagc agcaggtgcg cgccgggcgc gatcgccttg gccagtttgt tggctaacag 78640 caggtcgagc atggacgcct cgtcgaccac gacgaggtcg gcgtccagcg ggttgtcccg 78700 gtcgtaggcg gcgtccccgc ccggctggag ttggagcagg cggtgcacgg tcgccgcgtc 78760 gtgtccggtg agctcggtca gccgcttcgc cgctcgtccc gtcggcgcgg cgaggatcac 78820 cttggccttt ttcgcctgag ctaatgcgat gatcgaccgc acggtgaagc tcttgccgca 78880 gcctggacct ccggtgagca cggcgacctt ctcggtcagg gccagcttga cggcgcgctc 78940 ctgcgcctcg gcgagttcgg caccggtagc gcggcgcaac cagtcgaggg ccttgtgcca 79000 atcgacgtcg gcgaagacgg gcatccggtc cgcgctggtg ttcagcagcc gggacagctg 79060 gttggccagg gcgacttcgg cgcggtggaa gggcacgagg tagatcgcga ccgtcggcac 79120 ctcgtcgtca tcggtgggga tctcctcgcg gaccacacct tcctcggtga cgagttcggc 79180 gaggcattcg atcaccagcc cggtgtcgac ggcgaggatc ttcaccgcct cggcgatcag 79240 ctcgttctcc ggcaggtagc agttgccgtc gccggtggac tccgacagcg tgaactgaag 79300 gcccgccttt acccgctgcg gggagtcgtg cgggattccc accgctttgg cgatggtgtc 79360 ggcggtcttg aaaccgattc cccacacgtc gcctgccagc cggtatggct cttccttgac 79420 ggtccggatc gcgtcgtcgt ggtactgctt gtagatcttc accgccagcg aggtcgagac 79480 gccgacgcct tgcaggaaga tcatcacctc cttgatcgcc ttctgctcct cccacgcgtc 79540 ggcgatcagc ttcgtccgct tcgggccgag cttggggacc tcgatcagcc gcgcgggttc 79600 ctgctcgatg acgtcgagcg cggcgacgcc gaagtggtcg acgatcttct cggcgagttt 79660 ggggccgatg cccttgatca ggccagaccc caggtagcgg cggatacctt gcacggtcgc 79720 aggcagcacg gtcgtgtagt cgtcgacgtg gaactgccgc ccgtactggg ggtgcgaccc 79780 ccaccggccg cgcatgcgca acgcctcgcc gggctgcgcg cccagcagcg cgccgacgac 79840 cgtcaccagg tcaccgcccc ggccggtgtc gatccgcgcg acggtgtagc cgctctcctc 79900 gttggcgaac gtgatccgct ccagcgtgcc ctccagcacc gcagtccacg tggccgactc 79960 ccgtcctttt tccaccgaca acacgtatca cgaacggctg tcaagcaaac cggcggtcac 80020 cacatgcagc ggcatctccc gaacgcctcg ggctccggcg tcagcgggtg ggcgttcgcg 80080 atgccttggt gcggccggtg ggagttgtag attttttcgt cctcgcgcag ggcctggagt 80140 aggtgccgct ggctccagat c 80161 2 2595 PRT Saccharopolyspora spinosa 2 Met Ser Glu Ala Gly Asn Leu Ile Ala Val Ile Gly Leu Ser Cys Arg 1 5 10 15 Leu Pro Gln Ala Pro Asp Pro Ala Ser Phe Trp Arg Leu Leu Arg Thr 20 25 30 Gly Thr Asp Ala Ile Thr Thr Val Pro Glu Gly Arg Trp Gly Asp Pro 35 40 45 Leu Pro Gly Arg Asp Ala Pro Lys Gly Pro Glu Trp Gly Gly Phe Leu 50 55 60 Ala Asp Val Asp Cys Phe Asp Pro Glu Phe Phe Gly Ile Ser Pro Arg 65 70 75 80 Glu Ala Ala Thr Val Asp Pro Gln Gln Arg Leu Ala Leu Glu Leu Ala 85 90 95 Trp Glu Ala Leu Glu Asp Ala Gly Ile Pro Ala Gly Glu Leu Arg Gly 100 105 110 Thr Ala Ala Gly Val Phe Met Gly Ala Ile Ser Asp Asp Tyr Ala Ala 115 120 125 Leu Leu Arg Glu Ser Pro Pro Glu Val Ala Ala Gln Tyr Arg Leu Thr 130 135 140 Gly Thr His Arg Ser Leu Ile Ala Asn Arg Val Ser Tyr Val Leu Gly 145 150 155 160 Leu Arg Gly Pro Ser Leu Thr Val Asp Ser Gly Gln Ser Ser Ser Leu 165 170 175 Val Gly Val His Leu Ala Ser Glu Ser Leu Arg Arg Gly Glu Cys Thr 180 185 190 Ile Ala Leu Ala Gly Gly Val Asn Leu Asn Leu Ala Ala Glu Ser Asn 195 200 205 Ser Ala Leu Met Asp Phe Gly Ala Leu Ser Pro Asp Gly Arg Cys Phe 210 215 220 Thr Phe Asp Val Arg Ala Asn Gly Tyr Val Arg Gly Glu Gly Gly Gly 225 230 235 240 Leu Val Val Leu Lys Lys Ala Asp Gln Ala His Ala Asp Gly Asp Arg 245 250 255 Ile Tyr Cys Leu Ile Arg Gly Ser Ala Val Asn Asn Asp Gly Gly Gly 260 265 270 Ala Gly Leu Thr Val Pro Ala Ala Asp Ala Gln Ala Glu Leu Leu Arg 275 280 285 Gln Ala Tyr Arg Asn Ala Gly Val Asp Pro Ala Ala Val Gln Tyr Val 290 295 300 Glu Leu His Gly Ser Ala Thr Arg Val Gly Asp Pro Val Glu Ala Ala 305 310 315 320 Ala Leu Gly Ala Val Leu Gly Ala Ala Arg Arg Pro Gly Asp Glu Leu 325 330 335 Arg Val Gly Ser Ala Lys Thr Asn Val Gly His Leu Glu Ala Ala Ala 340 345 350 Gly Val Thr Gly Leu Leu Lys Thr Ala Leu Ser Ile Trp His Arg Glu 355 360 365 Leu Pro Pro Ser Leu His Phe Thr Ala Pro Asn Pro Glu Ile Pro Leu 370 375 380 Asp Glu Leu Asn Leu Arg Val Gln Arg Asp Leu Arg Pro Trp Pro Glu 385 390 395 400 Ser Glu Gly Pro Leu Leu Ala Gly Val Ser Ala Phe Gly Met Gly Gly 405 410 415 Thr Asn Cys His Leu Val Leu Ser Gly Thr Ser Arg Val Glu Arg Arg 420 425 430 Arg Ser Gly Pro Ala Glu Ala Thr Met Pro Trp Val Leu Ser Ala Arg 435 440 445 Thr Pro Val Ala Leu Arg Ala Gln Ala Ala Arg Leu His Thr His Leu 450 455 460 Asn Thr Ala Gly Gln Ser Pro Leu Asp Val Ala Tyr Ser Leu Ala Thr 465 470 475 480 Thr Arg Ser Ala Leu Pro His Arg Ala Ala Leu Val Ala Asp Asp Glu 485 490 495 Pro Lys Leu Leu Ala Gly Leu Lys Ala Leu Ala Asp Gly Asp Asp Ala 500 505 510 Pro Thr Leu Cys His Gly Ala Thr Ser Gly Glu Arg Ala Ala Val Phe 515 520 525 Val Phe Pro Gly Gln Gly Ser Gln Trp Ile Gly Met Gly Arg Gln Leu 530 535 540 Leu Glu Thr Ser Glu Val Phe Ala Ala Ser Met Ser Asp Cys Ala Asp 545 550 555 560 Ala Leu Ala Pro His Leu Asp Trp Ser Leu Leu Asp Val Leu Arg Asn 565 570 575 Ala Ala Gly Ala Ala His Leu Asp His Asp Asp Val Val Gln Pro Ala 580 585 590 Leu Phe Ala Ile Met Val Ser Leu Ala Glu Leu Trp Arg Ser Trp Gly 595 600 605 Val Arg Pro Val Ala Val Val Gly His Ser Gln Gly Glu Ile Ala Ala 610 615 620 Ala Cys Val Ala Gly Ala Leu Ser Val Arg Asp Ala Ala Arg Val Val 625 630 635 640 Ala Val Arg Ser Arg Leu Leu Thr Ala Leu Ala Gly Ser Gly Ala Met 645 650 655 Ala Ser Leu Gln His Pro Ala Glu Glu Val Arg Gln Ile Leu Leu Pro 660 665 670 Trp Arg Asp Arg Ile Gly Val Ala Gly Val Asn Gly Pro Ser Ser Thr 675 680 685 Leu Val Ser Gly Asp Arg Glu Ala Met Ala Glu Leu Leu Ala Glu Cys 690 695 700 Ala Asp Arg Glu Leu Arg Met Arg Arg Ile Pro Val Glu Tyr Ala Ser 705 710 715 720 His Ser Pro His Ile Glu Val Val Arg Asp Glu Leu Leu Gly Leu Leu 725 730 735 Ala Pro Val Glu Pro Arg Thr Gly Ser Ile Pro Ile Tyr Ser Thr Thr 740 745 750 Thr Gly Asp Leu Leu Asp Arg Pro Met Asp Ala Asp Tyr Trp Tyr Arg 755 760 765 Asn Leu Arg Gln Pro Val Leu Phe Glu Ala Ala Val Glu Ala Leu Leu 770 775 780 Lys Arg Gly Tyr Asp Ala Phe Ile Glu Ile Ser Pro His Pro Val Leu 785 790 795 800 Thr Ala Asn Ile Gln Glu Thr Ala Val Arg Ala Gly Arg Glu Val Val 805 810 815 Ala Leu Gly Thr Leu Arg Arg Gly Glu Gly Gly Met Arg Gln Ala Leu 820 825 830 Thr Ser Leu Ala Arg Ala His Val His Gly Val Ala Ala Asp Trp His 835 840 845 Ala Val Phe Ala Gly Thr Gly Ala Gln Arg Val Asp Leu Pro Thr Tyr 850 855 860 Ala Phe Gln Arg Gln Arg Tyr Trp Leu Asp Ala Lys Leu Pro Asp Val 865 870 875 880 Ala Met Pro Glu Ser Asp Val Ser Thr Ala Leu Arg Glu Lys Leu Arg 885 890 895 Ser Ser Pro Arg Ala Asp Val Asp Ser Thr Thr Leu Thr Met Ile Arg 900 905 910 Ala Gln Ala Ala Val Val Leu Gly His Ser Asp Pro Lys Glu Val Asp 915 920 925 Pro Asp Arg Thr Phe Lys Asp Leu Gly Phe Asp Ser Ser Met Val Val 930 935 940 Glu Leu Cys Asp Arg Leu Asn Ala Ala Thr Gly Leu Arg Leu Ala Pro 945 950 955 960 Ser Val Val Phe Asp Cys Pro Thr Pro Asp Lys Leu Ala Arg Gln Val 965 970 975 Arg Thr Leu Leu Leu Gly Glu Pro Ala Pro Met Thr Ser His Arg Pro 980 985 990 Asp Ser Asp Ala Asp Glu Pro Ile Ala Val Ile Gly Met Gly Cys Arg 995 1000 1005 Phe Pro Gly Gly Val Ser Ser Pro Glu Glu Leu Trp Gln Leu Val Ala 1010 1015 1020 Ala Gly Arg Asp Val Val Ser Glu Phe Pro Ala Asp Arg Gly Trp Asp 1025 1030 1035 1040 Leu Glu Arg Ala Gly Thr Ser His Val Arg Ala Gly Gly Phe Leu His 1045 1050 1055 Gly Ala Pro Asp Phe Asp Pro Gly Phe Phe Arg Ile Ser Pro Arg Glu 1060 1065 1070 Ala Leu Ala Met Asp Pro Gln Gln Arg Leu Leu Leu Glu Ile Ala Trp 1075 1080 1085 Glu Ala Val Glu Arg Gly Gly Ile Asn Pro Gln His Leu His Gly Ser 1090 1095 1100 Gln Thr Gly Val Phe Val Gly Ala Thr Ser Leu Asp Tyr Gly Pro Arg 1105 1110 1115 1120 Leu His Glu Ala Ser Glu Glu Ala Ala Gly Tyr Val Leu Thr Gly Ser 1125 1130 1135 Thr Thr Ser Val Ala Ser Gly Arg Val Ala Tyr Ser Phe Gly Phe Glu 1140 1145 1150 Gly Pro Ala Val Thr Val Asp Thr Ala Cys Ser Ser Ser Leu Val Ala 1155 1160 1165 Leu His Leu Ala Cys Gln Ser Leu Arg Ser Gly Glu Cys Asp Leu Ala 1170 1175 1180 Leu Ala Gly Gly Val Thr Val Met Ala Thr Pro Gly Met Phe Val Glu 1185 1190 1195 1200 Phe Ser Arg Gln Arg Gly Leu Ala Pro Asp Gly Arg Cys Lys Ser Phe 1205 1210 1215 Ala Glu Ala Ala Asp Gly Thr Gly Trp Ser Glu Gly Ala Gly Leu Val 1220 1225 1230 Leu Leu Glu Arg Leu Ser Asp Ala Arg Arg Asn Gly His Glu Val Leu 1235 1240 1245 Ala Val Val Arg Gly Ser Ala Val Asn Gln Asp Gly Ala Ser Asn Gly 1250 1255 1260 Leu Thr Ala Pro Asn Gly Ser Ser Gln Gln Arg Val Ile Ala Gln Ala 1265 1270 1275 1280 Leu Ala Ser Ala Gly Leu Ser Val Ser Asp Val Asp Ala Val Glu Ala 1285 1290 1295 His Gly Thr Gly Thr Arg Leu Gly Asp Pro Ile Glu Ala Gln Ala Leu 1300 1305 1310 Ile Ala Thr Tyr Gly Gln Gly Arg Leu Pro Glu Arg Pro Leu Trp Leu 1315 1320 1325 Gly Ser Met Lys Ser Asn Ile Gly His Ala Gln Ala Ala Ala Gly Ile 1330 1335 1340 Ala Gly Val Met Lys Met Val Met Ala Met Arg His Gly Gln Leu Pro 1345 1350 1355 1360 Arg Thr Leu His Val Asp Glu Pro Thr Ser Gly Val Asp Trp Ser Ala 1365 1370 1375 Gly Thr Val Gln Leu Leu Thr Glu Asn Thr Pro Trp Pro Gly Ser Gly 1380 1385 1390 Arg Val Arg Arg Val Gly Val Ser Ser Phe Gly Ile Ser Gly Thr Asn 1395 1400 1405 Ala His Val Ile Leu Glu Gln Pro Pro Gly Val Pro Ser Gln Ser Ala 1410 1415 1420 Gly Pro Gly Ser Gly Ser Val Val Asp Val Pro Val Val Pro Trp Met 1425 1430 1435 1440 Val Ser Gly Lys Thr Pro Glu Ala Leu Ser Ala Gln Ala Thr Ala Leu 1445 1450 1455 Met Thr Tyr Leu Asp Glu Arg Pro Asp Val Ser Ser Leu Asp Val Gly 1460 1465 1470 Tyr Ser Leu Ala Leu Thr Arg Ser Ala Leu Asp Glu Arg Ala Val Val 1475 1480 1485 Leu Gly Ser Asp Arg Glu Thr Leu Leu Cys Gly Val Lys Ala Leu Ser 1490 1495 1500 Ala Gly His Glu Ala Ser Gly Leu Val Thr Gly Ser Val Gly Ala Gly 1505 1510 1515 1520 Gly Arg Ile Gly Phe Val Phe Ser Gly Gln Gly Gly Gln Trp Leu Gly 1525 1530 1535 Met Gly Arg Gly Leu Tyr Arg Ala Phe Pro Val Phe Ala Ala Ala Phe 1540 1545 1550 Asp Glu Ala Cys Ala Glu Leu Asp Ala His Leu Gly Gln Glu Ile Gly 1555 1560 1565 Val Arg Glu Val Val Ser Gly Ser Asp Ala Gln Leu Leu Asp Arg Thr 1570 1575 1580 Leu Trp Ala Gln Ser Gly Leu Phe Ala Leu Gln Val Gly Leu Leu Lys 1585 1590 1595 1600 Leu Leu Asp Ser Trp Gly Val Arg Pro Ser Val Val Leu Gly His Ser 1605 1610 1615 Val Gly Glu Leu Ala Ala Ala Phe Ala Ala Gly Val Val Ser Leu Ser 1620 1625 1630 Gly Ala Ala Arg Leu Val Ala Gly Arg Ala Arg Leu Met Gln Ala Leu 1635 1640 1645 Pro Ser Gly Gly Gly Met Leu Ala Val Pro Ala Gly Glu Glu Leu Leu 1650 1655 1660 Trp Ser Leu Leu Ala Asp Gln Gly Asp Arg Val Gly Ile Ala Ala Val 1665 1670 1675 1680 Asn Ala Ala Gly Ser Val Val Leu Ser Gly Asp Arg Asp Val Leu Asp 1685 1690 1695 Asp Leu Ala Gly Arg Leu Asp Gly Gln Gly Ile Arg Ser Arg Trp Leu 1700 1705 1710 Arg Val Ser His Ala Phe His Ser Tyr Arg Met Asp Pro Met Leu Ala 1715 1720 1725 Glu Phe Ala Glu Leu Ala Arg Thr Val Asp Tyr Arg Arg Cys Glu Val 1730 1735 1740 Pro Ile Val Ser Thr Leu Thr Gly Asp Leu Asp Asp Ala Gly Arg Met 1745 1750 1755 1760 Ser Gly Pro Asp Tyr Trp Val Arg Gln Val Arg Glu Pro Val Arg Phe 1765 1770 1775 Ala Asp Gly Val Gln Ala Leu Val Glu His Asp Val Ala Thr Val Val 1780 1785 1790 Glu Leu Gly Pro Asp Gly Ala Leu Ser Ala Leu Ile Gln Glu Cys Val 1795 1800 1805 Ala Ala Ser Asp His Ala Gly Arg Leu Ser Ala Val Pro Ala Met Arg 1810 1815 1820 Arg Asn Gln Asp Glu Ala Gln Lys Val Met Thr Ala Leu Ala His Val 1825 1830 1835 1840 His Val Arg Gly Gly Ala Val Asp Trp Arg Ser Phe Phe Ala Gly Thr 1845 1850 1855 Arg Ala Lys Gln Ile Glu Leu Pro Thr Tyr Ala Phe Gln Arg Gln Arg 1860 1865 1870 Tyr Trp Leu Asn Ala Leu Arg Glu Ser Ser Ala Gly Asp Met Gly Arg 1875 1880 1885 Arg Val Glu Ala Lys Phe Trp Gly Ala Val Glu His Glu Asp Val Glu 1890 1895 1900 Ser Leu Ala Arg Val Leu Gly Ile Val Asp Asp Gly Ala Ala Val Asp 1905 1910 1915 1920 Ser Leu Arg Ser Ala Leu Pro Val Leu Ala Gly Trp Gln Arg Thr Arg 1925 1930 1935 Thr Thr Glu Ser Ile Met Asp Pro Arg Cys Tyr Arg Ile Gly Trp Arg 1940 1945 1950 Gln Val Ala Gly Leu Pro Pro Met Gly Thr Val Phe Gly Thr Trp Leu 1955 1960 1965 Val Phe Ala Pro His Gly Trp Ser Ser Glu Pro Glu Val Val Asp Cys 1970 1975 1980 Val Thr Ala Leu Arg Ala Arg Gly Ala Ser Val Val Leu Val Glu Ala 1985 1990 1995 2000 Asp Pro Asp Pro Thr Ser Phe Gly Asp Arg Val Arg Thr Leu Cys Ser 2005 2010 2015 Gly Leu Pro Asp Leu Val Gly Val Leu Ser Met Leu Cys Leu Glu Glu 2020 2025 2030 Ser Val Leu Pro Gly Phe Ser Ala Val Ser Arg Gly Phe Ala Leu Thr 2035 2040 2045 Val Glu Leu Val Arg Val Leu Arg Ala Ala Gly Ala Thr Ala Arg Leu 2050 2055 2060 Trp Leu Leu Thr Cys Gly Gly Val Ser Val Gly Asp Val Pro Val Arg 2065 2070 2075 2080 Pro Ala Gln Ala Leu Ala Trp Gly Leu Gly Arg Val Val Gly Leu Glu 2085 2090 2095 His Pro Asp Trp Trp Gly Gly Leu Ile Asp Ile Pro Val Leu Phe Asp 2100 2105 2110 Glu Asp Ala Gln Glu Arg Leu Ser Ile Val Leu Ala Gly Leu Asp Glu 2115 2120 2125 Asp Glu Val Ala Ile Arg Pro Asp Gly Met Phe Ala Arg Arg Leu Val 2130 2135 2140 Arg His Thr Val Ser Ala Asp Val Lys Lys Ala Trp Arg Pro Arg Gly 2145 2150 2155 2160 Ser Val Leu Val Thr Gly Gly Thr Gly Gly Leu Gly Ala His Val Ala 2165 2170 2175 Arg Trp Leu Ala Asp Ala Gly Ala Glu His Val Ala Met Val Ser Arg 2180 2185 2190 Arg Gly Glu Gln Ala Pro Ser Ala Glu Lys Leu Arg Thr Glu Leu Glu 2195 2200 2205 Asp Leu Gly Thr Arg Val Ser Ile Val Ser Cys Asp Val Thr Asp Arg 2210 2215 2220 Glu Ala Leu Ala Glu Val Leu Lys Ala Leu Pro Ala Glu Asn Pro Leu 2225 2230 2235 2240 Thr Ala Val Val His Ala Ala Gly Val Ile Glu Thr Gly Asp Ala Ala 2245 2250 2255 Ala Met Ser Leu Ala Asp Phe Asp His Val Leu Ser Ala Lys Val Ala 2260 2265 2270 Gly Ala Ala Asn Leu Asp Ala Leu Leu Ala Asp Val Glu Leu Asp Ala 2275 2280 2285 Phe Val Leu Phe Ser Ser Val Ser Gly Val Trp Gly Ala Gly Gly His 2290 2295 2300 Gly Ala Tyr Ala Ala Ala Asn Ala Tyr Leu Asp Ala Leu Ala Glu Gln 2305 2310 2315 2320 Arg Arg Ser Arg Gly Leu Val Ala Thr Ala Val Ala Trp Gly Pro Trp 2325 2330 2335 Ala Gly Glu Gly Met Ala Ser Gly Glu Thr Gly Asp Gln Leu Arg Arg 2340 2345 2350 Tyr Gly Leu Ser Pro Met Ala Pro Gln His Ala Ile Ala Gly Ile Arg 2355 2360 2365 Gln Ala Val Glu Gln Asp Glu Ile Ser Leu Val Val Ala Asp Val Asp 2370 2375 2380 Trp Ala Arg Phe Ser Ala Gly Leu Leu Ala Ala Arg Pro Arg Pro Leu 2385 2390 2395 2400 Leu Asn Glu Leu Ala Glu Val Lys Glu Leu Leu Val Asp Ala Gln Pro 2405 2410 2415 Glu Ala Gly Val Leu Ala Asp Ala Ser Leu Glu Trp Arg Gln Arg Leu 2420 2425 2430 Ser Ala Ala Pro Arg Pro Thr Gln Glu Gln Leu Ile Leu Glu Leu Val 2435 2440 2445 Arg Gly Glu Thr Ala Leu Val Leu Gly His Pro Gly Ala Ala Ala Val 2450 2455 2460 Ala Ser Glu Arg Ala Phe Lys Asp Ser Gly Phe Asp Ser Gln Ala Ala 2465 2470 2475 2480 Val Glu Leu Arg Val Arg Leu Asn Arg Ala Thr Gly Leu Gln Leu Pro 2485 2490 2495 Ser Thr Ile Ile Phe Ser His Pro Thr Pro Ala Glu Leu Ala Ala Glu 2500 2505 2510 Leu Arg Ala Arg Leu Leu Pro Glu Ser Ala Gly Ala Gly Ile Pro Glu 2515 2520 2525 Glu Asp Glu Ala Arg Ile Arg Ala Ala Leu Thr Ser Ile Pro Phe Pro 2530 2535 2540 Ala Leu Arg Glu Ala Gly Leu Val Ser Pro Leu Leu Ala Leu Ala Gly 2545 2550 2555 2560 His Pro Val Asp Ser Gly Ile Ser Ser Asp Asp Ala Ala Ala Thr Ser 2565 2570 2575 Ile Asp Ala Met Asp Val Ala Gly Leu Val Glu Ala Ala Leu Gly Glu 2580 2585 2590 Arg Glu Ser 2595 3 2152 PRT Saccharopolyspora spinosa 3 Met Thr Val Thr Thr Ser Tyr Glu Glu Val Val Glu Ala Leu Arg Ala 1 5 10 15 Ser Leu Lys Glu Asn Glu Arg Leu Arg Arg Gly Arg Asp Arg Phe Ser 20 25 30 Ala Glu Lys Asp Asp Pro Ile Ala Ile Val Ala Met Ser Cys Arg Tyr 35 40 45 Pro Gly Gln Val Ser Ser Pro Glu Asp Leu Trp Gln Leu Ala Ala Gly 50 55 60 Gly Val Asp Ala Ile Ser Glu Val Pro Gly Asp Arg Gly Trp Asp Leu 65 70 75 80 Asp Gly Val Phe Val Pro Asp Ser Asp Arg Pro Gly Thr Ser Tyr Ala 85 90 95 Cys Ala Gly Gly Phe Leu Gln Gly Val Ser Glu Phe Asp Ala Gly Phe 100 105 110 Phe Gly Ile Ser Pro Arg Glu Ala Leu Ala Met Asp Pro Gln Gln Arg 115 120 125 Leu Leu Leu Glu Val Ala Trp Glu Val Phe Glu Arg Ala Gly Leu Glu 130 135 140 Gln Arg Ser Thr Arg Gly Ser Arg Val Gly Val Phe Val Gly Thr Asn 145 150 155 160 Gly Gln Asp Tyr Ala Ser Trp Leu Arg Thr Pro Pro Pro Ala Val Ala 165 170 175 Gly His Val Leu Thr Gly Gly Ala Ala Ala Val Leu Ser Gly Arg Val 180 185 190 Ala Tyr Ser Phe Gly Phe Glu Gly Pro Ala Val Thr Val Asp Thr Ala 195 200 205 Cys Ser Ser Ser Leu Val Ala Leu His Leu Ala Gly Gln Ala Leu Arg 210 215 220 Ala Gly Glu Cys Asp Leu Ala Leu Ala Gly Gly Val Thr Val Met Ser 225 230 235 240 Thr Pro Lys Val Phe Leu Glu Phe Ser Arg Gln Arg Gly Leu Ala Pro 245 250 255 Asp Gly Arg Cys Lys Ser Phe Ala Ala Gly Ala Asp Gly Thr Gly Trp 260 265 270 Gly Glu Gly Ala Gly Leu Leu Leu Leu Glu Arg Leu Ser Asp Ala Arg 275 280 285 Arg Asn Gly His Glu Val Leu Ala Val Val Arg Gly Ser Ala Val Asn 290 295 300 Gln Asp Gly Ala Ser Asn Gly Leu Thr Ala Pro Asn Gly Ser Ser Gln 305 310 315 320 Gln Arg Val Ile Thr Gln Ala Leu Ala Ser Ala Gly Leu Ser Val Ser 325 330 335 Asp Val Asp Ala Val Glu Ala His Gly Thr Gly Thr Arg Leu Gly Asp 340 345 350 Pro Ile Glu Ala Gln Ala Leu Ile Ala Thr Tyr Gly Arg Asp Arg Asp 355 360 365 Pro Gly Arg Pro Leu Trp Leu Gly Ser Val Lys Ser Asn Ile Gly His 370 375 380 Thr Gln Ala Ala Ala Gly Val Ala Gly Val Ile Lys Met Val Met Ala 385 390 395 400 Met Arg His Gly Gln Leu Pro Arg Thr Leu His Val Glu Ser Pro Ser 405 410 415 Pro Glu Val Asp Trp Ser Ala Gly Thr Val Gln Leu Leu Thr Glu Asn 420 425 430 Thr Pro Trp Pro Arg Ser Gly Arg Val Arg Arg Val Gly Val Ser Ser 435 440 445 Phe Gly Ile Ser Gly Thr Asn Ala His Val Ile Leu Glu Gln Pro Pro 450 455 460 Gly Val Pro Ser Gln Ser Ala Gly Pro Gly Ser Gly Ser Val Val Asp 465 470 475 480 Val Pro Val Val Pro Trp Met Val Ser Gly Lys Thr Pro Glu Ala Leu 485 490 495 Ser Ala Gln Ala Thr Ala Leu Met Thr Tyr Leu Asp Glu Arg Pro Asp 500 505 510 Val Ser Ser Leu Asp Val Gly Tyr Ser Leu Ala Leu Thr Arg Ser Ala 515 520 525 Leu Asp Glu Arg Ala Val Val Leu Gly Ser Asp Arg Glu Thr Leu Leu 530 535 540 Cys Gly Val Lys Ala Leu Ser Ala Gly His Glu Ala Ser Gly Leu Val 545 550 555 560 Thr Gly Ser Val Gly Ala Gly Gly Arg Ile Gly Phe Val Phe Ser Gly 565 570 575 Gln Gly Gly Gln Trp Leu Gly Met Gly Arg Gly Leu Tyr Arg Ala Phe 580 585 590 Pro Val Phe Ala Ala Ala Phe Asp Glu Ala Cys Ala Glu Leu Asp Ala 595 600 605 His Leu Gly Gln Glu Ile Gly Val Arg Glu Val Val Ser Gly Ser Asp 610 615 620 Ala Gln Leu Leu Asp Arg Thr Leu Trp Ala Gln Ser Gly Leu Phe Ala 625 630 635 640 Leu Gln Val Gly Leu Leu Lys Leu Leu Asp Ser Trp Gly Val Arg Pro 645 650 655 Ser Val Val Leu Gly His Ser Val Gly Glu Leu Ala Ala Ala Phe Ala 660 665 670 Ala Gly Val Val Ser Leu Ser Gly Ala Ala Arg Leu Val Ala Gly Arg 675 680 685 Ala Arg Leu Met Gln Ala Leu Pro Ser Gly Gly Gly Met Leu Ala Val 690 695 700 Pro Ala Gly Glu Glu Leu Leu Trp Ser Leu Leu Ala Asp Gln Gly Asp 705 710 715 720 Arg Val Gly Ile Ala Ala Val Asn Ala Ala Gly Ser Val Val Leu Ser 725 730 735 Gly Asp Arg Asp Val Leu Asp Asp Leu Ala Gly Arg Leu Asp Gly Gln 740 745 750 Gly Ile Arg Ser Arg Trp Leu Arg Val Ser His Ala Phe His Ser Tyr 755 760 765 Arg Met Asp Pro Met Leu Ala Glu Phe Ala Glu Leu Ala Arg Thr Val 770 775 780 Asp Tyr Arg Arg Cys Glu Val Pro Ile Val Ser Thr Leu Thr Gly Asp 785 790 795 800 Leu Asp Asp Ala Gly Arg Met Ser Gly Pro Asp Tyr Trp Val Arg Gln 805 810 815 Val Arg Glu Pro Val Arg Phe Ala Asp Gly Val Gln Ala Leu Val Glu 820 825 830 His Asp Val Ala Thr Val Val Glu Leu Gly Pro Asp Gly Ala Leu Ser 835 840 845 Ala Leu Ile Gln Glu Cys Val Ala Ala Ser Asp His Ala Gly Arg Leu 850 855 860 Ser Ala Val Pro Ala Met Arg Arg Asn Gln Asp Glu Ala Gln Lys Val 865 870 875 880 Met Thr Ala Leu Ala His Val His Val Arg Gly Gly Ala Val Asp Trp 885 890 895 Arg Ser Phe Phe Ala Gly Thr Gly Ala Lys Gln Ile Glu Leu Pro Thr 900 905 910 Tyr Ala Phe Gln Arg Gln Arg Tyr Trp Leu Val Pro Ser Asp Ser Gly 915 920 925 Asp Val Thr Gly Ala Gly Leu Ala Gly Ala Glu His Pro Leu Leu Gly 930 935 940 Ala Val Val Pro Val Ala Gly Gly Asp Glu Val Leu Leu Thr Gly Arg 945 950 955 960 Ile Ser Val Arg Thr His Pro Trp Leu Ala Glu His Arg Val Leu Gly 965 970 975 Glu Val Ile Val Ala Gly Thr Ala Leu Leu Glu Ile Ala Leu His Ala 980 985 990 Gly Glu Arg Leu Gly Cys Glu Arg Val Glu Glu Leu Thr Leu Glu Ala 995 1000 1005 Pro Leu Val Leu Pro Glu Arg Gly Ala Ile Gln Val Gln Leu Arg Val 1010 1015 1020 Gly Ala Pro Glu Asn Ser Gly Arg Arg Pro Met Ala Leu Tyr Ser Arg 1025 1030 1035 1040 Pro Glu Gly Ala Ala Glu His Asp Trp Thr Arg His Ala Thr Gly Arg 1045 1050 1055 Leu Ala Pro Gly Arg Gly Glu Ala Ala Gly Asp Leu Ala Asp Trp Pro 1060 1065 1070 Ala Pro Gly Ala Leu Pro Val Asp Leu Asp Glu Phe Tyr Arg Asp Leu 1075 1080 1085 Ala Glu Leu Gly Leu Glu Tyr Gly Pro Ile Phe Gln Gly Leu Lys Ala 1090 1095 1100 Ala Trp Arg Gln Gly Asp Glu Val Tyr Ala Glu Ala Ala Leu Pro Gly 1105 1110 1115 1120 Thr Glu Asp Ser Gly Phe Gly Val His Pro Ala Leu Leu Asp Ala Ala 1125 1130 1135 Leu His Ala Thr Ala Val Arg Asp Met Asp Asp Ala Arg Leu Pro Phe 1140 1145 1150 Gln Trp Glu Gly Val Ser Leu His Ala Lys Ala Ala Pro Ala Leu Arg 1155 1160 1165 Val Arg Val Val Pro Ala Gly Asp Asp Ala Lys Ser Leu Leu Val Cys 1170 1175 1180 Asp Gly Thr Gly Arg Pro Val Ile Ser Val Asp Arg Leu Val Leu Arg 1185 1190 1195 1200 Ser Ala Ala Ala Arg Arg Thr Gly Ala Arg Arg Gln Ala His Gln Ala 1205 1210 1215 Arg Leu Tyr Arg Leu Ser Trp Pro Thr Val Gln Leu Pro Thr Ser Ala 1220 1225 1230 Gln Pro Pro Ser Cys Val Leu Leu Gly Thr Ser Glu Val Ser Ala Asp 1235 1240 1245 Ile Gln Val Tyr Pro Asp Leu Arg Ser Leu Thr Ala Ala Leu Asp Ala 1250 1255 1260 Gly Ala Glu Pro Pro Gly Val Val Ile Ala Pro Thr Pro Pro Gly Gly 1265 1270 1275 1280 Gly Arg Thr Ala Asp Val Arg Glu Thr Thr Arg His Ala Leu Asp Leu 1285 1290 1295 Val Gln Gly Trp Leu Ser Asp Gln Arg Leu Asn Glu Ser Arg Leu Leu 1300 1305 1310 Leu Val Thr Gln Gly Ala Val Ala Val Glu Pro Gly Glu Pro Val Thr 1315 1320 1325 Asp Leu Ala Gln Ala Ala Leu Trp Gly Leu Leu Arg Ser Thr Gln Thr 1330 1335 1340 Glu His Pro Asp Arg Phe Val Leu Val Asp Val Pro Glu Pro Ala Gln 1345 1350 1355 1360 Leu Leu Pro Ala Leu Pro Gly Val Leu Ala Cys Gly Glu Pro Gln Leu 1365 1370 1375 Ala Leu Arg Arg Gly Gly Ala His Ala Pro Arg Leu Ala Gly Leu Gly 1380 1385 1390 Ser Asp Asp Val Leu Pro Val Pro Asp Gly Thr Gly Trp Arg Leu Glu 1395 1400 1405 Ala Thr Arg Pro Gly Ser Leu Asp Gly Leu Ala Leu Val Asp Glu Pro 1410 1415 1420 Thr Ala Thr Ala Pro Leu Gly Asp Gly Glu Val Arg Ile Ala Met Arg 1425 1430 1435 1440 Ala Ala Gly Val Asn Phe Arg Asp Ala Leu Ile Ala Leu Gly Met Tyr 1445 1450 1455 Pro Gly Val Ala Ser Leu Gly Ser Glu Gly Ala Gly Val Val Val Glu 1460 1465 1470 Thr Gly Pro Gly Val Thr Gly Leu Ala Pro Gly Asp Arg Val Met Gly 1475 1480 1485 Met Ile Pro Lys Ala Phe Gly Pro Leu Ala Val Ala Asp His Arg Met 1490 1495 1500 Val Thr Arg Ile Pro Ala Gly Trp Ser Phe Ala Arg Ala Ala Ser Val 1505 1510 1515 1520 Pro Ile Val Phe Leu Thr Ala Tyr Tyr Ala Leu Val Asp Leu Ala Gly 1525 1530 1535 Leu Arg Pro Gly Glu Ser Leu Leu Val His Ser Ala Ala Gly Gly Val 1540 1545 1550 Gly Met Ala Ala Ile Gln Leu Ala Arg His Leu Gly Ala Glu Val Tyr 1555 1560 1565 Ala Thr Ala Ser Glu Asp Lys Trp Gln Ala Val Glu Leu Ser Arg Glu 1570 1575 1580 His Leu Ala Ser Ser Arg Thr Cys Asp Phe Glu Gln Gln Phe Leu Gly 1585 1590 1595 1600 Ala Thr Gly Gly Arg Gly Val Asp Val Val Leu Asn Ser Leu Ala Gly 1605 1610 1615 Glu Phe Ala Asp Ala Ser Leu Arg Met Leu Pro Arg Gly Gly Arg Phe 1620 1625 1630 Leu Glu Leu Gly Lys Thr Asp Val Arg Asp Pro Val Glu Val Ala Asp 1635 1640 1645 Ala His Pro Gly Val Ser Tyr Gln Ala Phe Asp Thr Val Glu Ala Gly 1650 1655 1660 Pro Gln Arg Ile Gly Glu Met Leu His Glu Leu Val Glu Leu Phe Glu 1665 1670 1675 1680 Gly Arg Val Leu Glu Pro Leu Pro Val Thr Ala Trp Asp Val Arg Gln 1685 1690 1695 Ala Pro Glu Ala Leu Arg His Leu Ser Gln Ala Arg His Val Gly Lys 1700 1705 1710 Leu Val Leu Thr Met Pro Pro Val Trp Asp Ala Ala Gly Thr Val Leu 1715 1720 1725 Val Thr Gly Gly Thr Gly Ala Leu Gly Ala Glu Val Ala Arg His Leu 1730 1735 1740 Val Ile Glu Arg Gly Val Arg Asn Leu Val Leu Val Ser Arg Arg Gly 1745 1750 1755 1760 Pro Ala Ala Ser Gly Ala Ala Glu Leu Val Ala Gln Leu Thr Ala Tyr 1765 1770 1775 Gly Ala Glu Val Ser Leu Gln Ala Cys Asp Val Ala Asp Arg Glu Thr 1780 1785 1790 Leu Ala Lys Val Leu Ala Ser Ile Pro Asp Glu His Pro Leu Thr Ala 1795 1800 1805 Val Val His Ala Ala Gly Val Leu Asp Asp Gly Val Ser Glu Ser Leu 1810 1815 1820 Thr Val Glu Arg Leu Asp Gln Val Leu Arg Pro Lys Val Asp Gly Ala 1825 1830 1835 1840 Arg Asn Leu Leu Glu Leu Ile Asp Pro Asp Val Ala Leu Val Leu Phe 1845 1850 1855 Ser Ser Val Ser Gly Val Leu Gly Ser Gly Gly Gln Gly Asn Tyr Ala 1860 1865 1870 Ala Ala Asn Ser Phe Leu Asp Ala Leu Ala Gln Gln Arg Gln Ser Arg 1875 1880 1885 Gly Leu Pro Thr Arg Ser Leu Ala Trp Gly Pro Trp Ala Glu His Gly 1890 1895 1900 Met Ala Ser Thr Leu Arg Glu Ala Glu Gln Asp Arg Leu Ala Arg Ser 1905 1910 1915 1920 Gly Leu Leu Pro Ile Ser Thr Glu Glu Gly Leu Ser Gln Phe Asp Ala 1925 1930 1935 Ala Cys Gly Gly Ala His Thr Val Val Ala Pro Val Arg Phe Ser Arg 1940 1945 1950 Leu Ser Asp Gly Asn Ala Ile Lys Phe Ser Val Leu Gln Gly Leu Val 1955 1960 1965 Gly Pro His Arg Val Asn Lys Ala Ala Thr Ala Asp Asp Ala Glu Ser 1970 1975 1980 Leu Arg Lys Arg Leu Gly Arg Leu Pro Asp Ala Glu Gln His Arg Ile 1985 1990 1995 2000 Leu Leu Asp Leu Val Arg Met His Val Ala Ala Val Leu Gly Phe Ala 2005 2010 2015 Gly Ser Gln Glu Ile Thr Ala Asp Gly Thr Phe Lys Val Leu Gly Phe 2020 2025 2030 Asp Ser Leu Thr Val Val Glu Leu Arg Asn Arg Ile Asn Gly Ala Thr 2035 2040 2045 Gly Leu Arg Leu Pro Ala Thr Leu Val Phe Asn Tyr Pro Thr Pro Asp 2050 2055 2060 Ala Leu Ala Ala His Leu Val Thr Ala Leu Ser Ala Asp Arg Leu Ala 2065 2070 2075 2080 Gly Thr Phe Glu Glu Leu Asp Arg Trp Ala Ala Asn Leu Pro Thr Leu 2085 2090 2095 Ala Arg Asp Glu Ala Thr Arg Ala Gln Ile Thr Thr Arg Leu Gln Ala 2100 2105 2110 Ile Leu Gln Ser Leu Ala Asp Val Ser Gly Gly Thr Gly Gly Gly Ser 2115 2120 2125 Val Pro Asp Arg Leu Arg Ser Ala Thr Asp Asp Glu Leu Phe Gln Leu 2130 2135 2140 Leu Asp Asn Asp Leu Glu Leu Pro 2145 2150 4 3170 PRT Saccharopolyspora spinosa 4 Met Ser Asn Glu Glu Lys Leu Arg Glu Tyr Leu Arg Arg Ala Leu Val 1 5 10 15 Asp Leu His Gln Ala Arg Glu Arg Leu His Glu Ala Glu Ser Gly Glu 20 25 30 Arg Glu Pro Ile Ala Ile Val Ala Met Gly Cys Arg Tyr Pro Gly Gly 35 40 45 Val Gln Asp Pro Glu Gly Leu Trp Lys Leu Val Ala Ser Gly Gly Asp 50 55 60 Ala Ile Gly Glu Phe Pro Ala Asp Arg Gly Trp His Leu Asp Glu Leu 65 70 75 80 Tyr Asp Pro Asp Pro Asp Gln Pro Gly Thr Cys Tyr Thr Arg His Gly 85 90 95 Gly Phe Leu His Asp Ala Gly Glu Phe Asp Ala Gly Phe Phe Asp Ile 100 105 110 Ser Pro Arg Glu Ala Leu Ala Met Asp Pro Gln Gln Arg Leu Leu Leu 115 120 125 Glu Ile Ser Trp Glu Thr Val Glu Ser Ala Gly Met Asp Pro Arg Ser 130 135 140 Leu Arg Gly Ser Arg Thr Gly Val Phe Ala Gly Leu Met Tyr Glu Gly 145 150 155 160 Tyr Asp Thr Gly Ala His Arg Ala Gly Glu Gly Val Glu Gly Tyr Leu 165 170 175 Gly Thr Gly Asn Ala Gly Ser Val Ala Ser Gly Arg Val Ala Tyr Ala 180 185 190 Phe Gly Phe Glu Gly Pro Ala Val Thr Val Asp Thr Ala Cys Ser Ser 195 200 205 Ser Leu Val Ala Leu His Leu Ala Cys Gln Ser Leu Arg Gln Gly Glu 210 215 220 Cys Asp Leu Ala Leu Ala Gly Gly Val Thr Val Met Ser Thr Pro Glu 225 230 235 240 Arg Phe Val Glu Phe Ser Arg Gln Arg Gly Leu Ala Pro Asp Gly Arg 245 250 255 Cys Lys Ser Phe Ala Ala Ala Ala Asp Gly Thr Gly Trp Gly Glu Gly 260 265 270 Ala Gly Leu Val Leu Leu Glu Arg Leu Ser Asp Ala Arg Arg Asn Gly 275 280 285 His Arg Val Leu Ala Val Val Arg Gly Ser Ala Val Asn Gln Asp Gly 290 295 300 Ala Ser Asn Gly Leu Thr Ala Pro Asn Gly Leu Ala Gln Glu Arg Val 305 310 315 320 Ile Gln Gln Val Leu Thr Ser Ala Gly Leu Ser Ala Ser Asp Val Asp 325 330 335 Ala Val Glu Ala His Gly Thr Gly Thr Arg Leu Gly Asp Pro Ile Glu 340 345 350 Ala Gln Ala Leu Ile Ala Ala Tyr Gly Gln Asp Arg Asp Arg Asp Arg 355 360 365 Pro Leu Trp Leu Gly Ser Val Lys Ser Asn Ile Gly His Thr Gln Ala 370 375 380 Ala Ala Gly Val Ala Gly Val Ile Lys Met Val Met Ala Met Arg His 385 390 395 400 Gly Glu Leu Pro Arg Thr Leu His Val Asp Glu Pro Asn Ser His Val 405 410 415 Asp Trp Ser Ala Gly Ala Val Arg Leu Leu Thr Glu Asn Ile Arg Trp 420 425 430 Pro Gly Thr Gly Thr Arg Arg Ala Gly Val Ser Ser Phe Gly Val Ser 435 440 445 Gly Thr Asn Ala His Val Ile Leu Glu His Asp Pro Leu Ala Val Thr 450 455 460 Glu Asn Glu Glu Ala Ala Gln Ser Pro Ala Pro Gly Ile Val Pro Trp 465 470 475 480 Ala Leu Ser Gly Arg Ser Ser Thr Ala Leu Arg Ala Gln Ala Glu Arg 485 490 495 Leu Arg Glu Leu Cys Glu Gln Thr Asp Pro Asp Pro Val Asp Val Gly 500 505 510 Phe Ser Leu Ala Ala Thr Arg Thr Ala Trp Glu His Arg Ala Val Val 515 520 525 Leu Gly Arg Asp Ser Ala Thr Leu Arg Ser Gly Leu Gly Val Val Ala 530 535 540 Ser Gly Glu Pro Ala Val Asp Val Val Glu Gly Ser Val Leu Asp Gly 545 550 555 560 Glu Val Val Phe Val Phe Pro Gly Gln Gly Trp Gln Trp Ala Gly Met 565 570 575 Ala Val Asp Leu Leu Asp Ala Ser Pro Thr Phe Ala Arg His Met Asp 580 585 590 Glu Cys Ala Thr Ala Leu Arg Arg Tyr Val Asp Trp Ser Leu Val Asp 595 600 605 Val Leu Arg Gly Ala Glu Asn Ser Pro Pro Leu Asp Arg Val Asp Val 610 615 620 Leu Gln Pro Ala Ser Phe Ala Val Met Val Ser Leu Ala Glu Val Trp 625 630 635 640 Arg Ser Tyr Gly Val Arg Pro Ala Ala Val Val Gly His Ser Gln Gly 645 650 655 Glu Ile Ala Ala Ala Cys Ala Ala Gly Val Leu Pro Leu Glu Asp Ala 660 665 670 Ala Arg Leu Val Ala Leu Arg Ser Arg Ala Leu Lys Gly Leu Ser Gly 675 680 685 Arg Gly Gly Met Ala Ser Leu Ala Cys Pro Ala Asp Glu Val Ala Ala 690 695 700 Leu Phe Ala Gly Ser Gly Gly Arg Leu Glu Val Ala Ala Ile Asn Gly 705 710 715 720 Pro Arg Ser Val Val Val Ser Gly Asp Leu Glu Ala Val Asp Glu Leu 725 730 735 Leu Ala Glu Cys Ala Glu Lys Asp Met Arg Ala Arg Arg Ile Pro Val 740 745 750 Asp Tyr Ala Ser His Ser Ala His Val Glu Val Val Arg Ser Pro Val 755 760 765 Leu Ala Ala Ala Ala Gly Val Arg His Arg Asp Gly Gln Val Pro Trp 770 775 780 Trp Ser Thr Val Ile Gly Asp Trp Val Asp Pro Ala Arg Leu Asp Gly 785 790 795 800 Glu Tyr Trp Tyr Arg Asn Leu Arg Gln Pro Val Arg Phe Glu His Ala 805 810 815 Val Gln Gly Leu Val Glu Arg Gly Phe Gly Leu Phe Ile Glu Met Ser 820 825 830 Ala His Pro Val Leu Thr Thr Ala Val Glu Glu Thr Gly Ala Glu Ser 835 840 845 Glu Thr Ala Val Ala Ala Val Gly Thr Leu Arg Arg Asp Ser Gly Gly 850 855 860 Leu Arg Arg Leu Leu His Ser Leu Ala Glu Ala Tyr Val Arg Gly Ala 865 870 875 880 Thr Val Asp Trp Ala Val Ala Phe Gly Gly Ala Gly Arg Arg Leu Asp 885 890 895 Leu Pro Thr Tyr Pro Phe Gln Arg Gln Arg Tyr Trp Leu Asp Lys Gly 900 905 910 Ala Ala Ser Asp Glu Ala Arg Ala Val Ser Asp Pro Ala Ala Gly Trp 915 920 925 Phe Trp Gln Ala Val Ala Arg Gln Asp Leu Lys Ser Val Ser Asp Ala 930 935 940 Leu Asp Leu Asp Ala Asp Ala Pro Leu Ser Ala Thr Leu Pro Ala Leu 945 950 955 960 Ser Val Trp His Arg Gln Glu Arg Glu Arg Val Leu Ala Asp Gly Trp 965 970 975 Arg Tyr Arg Val Asp Trp Val Arg Val Ala Pro Gln Pro Val Arg Arg 980 985 990 Thr Arg Glu Thr Trp Leu Leu Val Val Pro Pro Gly Gly Ile Glu Glu 995 1000 1005 Ala Leu Val Glu Arg Leu Thr Asp Ala Leu Asn Thr Arg Gly Ile Ser 1010 1015 1020 Thr Leu Arg Leu Asp Val Pro Pro Ala Ala Thr Ser Gly Glu Leu Ala 1025 1030 1035 1040 Thr Glu Leu Arg Ala Ala Ala Asp Gly Asp Pro Val Lys Ala Ile Leu 1045 1050 1055 Ser Leu Thr Ala Leu Asp Glu Arg Pro His Pro Glu Cys Lys Asp Val 1060 1065 1070 Pro Ser Gly Ile Ala Leu Leu Leu Asn Leu Val Lys Ala Leu Gly Glu 1075 1080 1085 Ala Asp Leu Arg Ile Pro Leu Trp Thr Ile Thr Arg Gly Ala Val Lys 1090 1095 1100 Ala Gly Pro Ala Asp Arg Leu Leu Arg Pro Met Gln Ala Gln Ala Trp 1105 1110 1115 1120 Gly Leu Gly Arg Val Ala Ala Leu Glu His Pro Glu Arg Trp Gly Gly 1125 1130 1135 Leu Ile Asp Leu Pro Asp Ser Leu Asp Gly Asp Val Leu Thr Arg Leu 1140 1145 1150 Gly Glu Ala Leu Thr Asn Gly Leu Ala Glu Asp Gln Leu Ala Ile Arg 1155 1160 1165 Gln Ser Gly Val Leu Ala Arg Arg Leu Val Pro Ala Pro Ala Asn Gln 1170 1175 1180 Pro Ala Gly Arg Lys Trp Arg Pro Arg Gly Ser Ala Leu Ile Thr Gly 1185 1190 1195 1200 Gly Leu Gly Ala Val Gly Ala Gln Val Ala Arg Trp Leu Ala Glu Ile 1205 1210 1215 Gly Ala Glu Arg Ile Val Leu Thr Ser Arg Arg Gly Asn Gln Ala Ala 1220 1225 1230 Gly Ala Ala Glu Leu Glu Ala Glu Leu Arg Ala Leu Gly Ala Gln Val 1235 1240 1245 Ser Ile Val Ala Cys Asp Val Thr Asp Arg Ala Glu Met Ser Ala Leu 1250 1255 1260 Leu Ala Glu Phe Asp Val Thr Ala Val Phe His Ala Ala Gly Val Gly 1265 1270 1275 1280 Arg Leu Leu Pro Leu Ala Glu Thr Asp Gln Asn Gly Leu Ala Glu Ile 1285 1290 1295 Cys Ala Ala Lys Val Arg Gly Ala Gln Val Leu Asp Glu Leu Cys Asp 1300 1305 1310 Ser Thr Asp Leu Asp Ala Phe Val Leu Phe Ser Ser Gly Ala Gly Val 1315 1320 1325 Trp Gly Gly Gly Gly Gln Gly Ala Tyr Gly Ala Ala Asn Ala Phe Leu 1330 1335 1340 Asp Thr Leu Ala Glu Gln Arg Arg Ala Arg Gly Leu Pro Ala Thr Ser 1345 1350 1355 1360 Ile Ser Trp Gly Ser Trp Ala Gly Gly Gly Met Ala Asp Gly Ala Ala 1365 1370 1375 Gly Glu His Leu Arg Arg Arg Gly Ile Arg Pro Met Pro Ala Ala Ser 1380 1385 1390 Ala Ile Leu Ala Leu Gln Glu Val Leu Asp Gln Asp Glu Thr Cys Val 1395 1400 1405 Ser Ile Ala Asp Val Asp Trp Asp Arg Phe Val Pro Thr Phe Ala Ala 1410 1415 1420 Thr Arg Ala Thr Arg Leu Phe Asp Glu Val Pro Ala Ala Arg Lys Ala 1425 1430 1435 1440 Met Pro Ala Asn Gly Pro Ala Glu Pro Gly Gly Ser Pro Phe Ala Arg 1445 1450 1455 Asn Leu Ala Glu Leu Pro Glu Ala Gln Arg Arg His Glu Leu Val Asp 1460 1465 1470 Leu Val Cys Ala Gln Val Ala Thr Val Leu Gly His Gly Ser Arg Glu 1475 1480 1485 Glu Val Gln Pro Glu Arg Ala Phe Arg Ala Leu Gly Phe Asp Ser Leu 1490 1495 1500 Met Ala Val Asp Leu Arg Asn Arg Leu Thr Thr Ala Thr Gly Leu Arg 1505 1510 1515 1520 Leu Pro Thr Thr Thr Val Phe Asp Tyr Pro Asn Pro Ala Ala Leu Ala 1525 1530 1535 Ala His Leu Leu Glu Glu Leu Val Gly Asp Val Ala Ser Ala Ala Val 1540 1545 1550 Thr Ala Ala Ser Ala Pro Ala Ser Asp Glu Pro Ile Ala Ile Val Ala 1555 1560 1565 Met Ser Cys Arg Phe Pro Gly Gly Ala His Ser Pro Glu Asp Leu Trp 1570 1575 1580 Arg Leu Val Ala Ala Gly Thr Glu Val Ile Gly Glu Phe Pro Ser Asp 1585 1590 1595 1600 Arg Gly Trp Asp Ala Glu Gly Leu Tyr Asp Pro Asp Ala Ser Arg Pro 1605 1610 1615 Gly Thr Thr Tyr Ala Arg Met Ala Gly Phe Leu Tyr Asp Ala Gly Glu 1620 1625 1630 Phe Asp Ala Asp Leu Phe Gly Ile Ser Pro Arg Glu Ala Leu Ala Met 1635 1640 1645 Asp Pro Gln Gln Arg Leu Val Leu Glu Ile Ala Trp Glu Ala Leu Glu 1650 1655 1660 Arg Ala Gly Ile Asp Pro Leu Ser Leu Lys Gly Ser Gly Val Gly Thr 1665 1670 1675 1680 Tyr Ile Gly Ala Gly Ser Arg Gly Tyr Ala Thr Asp Val Arg Gln Phe 1685 1690 1695 Pro Glu Glu Ala Glu Gly Tyr Leu Leu Thr Gly Thr Ser Ala Ser Val 1700 1705 1710 Leu Ser Gly Arg Val Ala Tyr Ser Phe Gly Phe Glu Gly Pro Ala Val 1715 1720 1725 Thr Val Asp Thr Ala Cys Ser Ser Ser Leu Val Ala Leu His Leu Ala 1730 1735 1740 Cys Gln Ser Leu Arg Ser Gly Glu Cys Asp Leu Ala Leu Ala Gly Gly 1745 1750 1755 1760 Val Thr Val Met Ser Thr Pro Glu Met Phe Val Glu Phe Ser Arg Gln 1765 1770 1775 Arg Gly Leu Ala Pro Asp Gly Arg Cys Lys Ser Phe Ala Glu Ser Ala 1780 1785 1790 Asp Gly Thr Gly Trp Gly Glu Gly Ala Gly Leu Leu Leu Leu Glu Arg 1795 1800 1805 Leu Ser Asp Ala His Arg Asn Gly His Arg Val Leu Ala Val Val Arg 1810 1815 1820 Gly Ser Ala Val Asn Gln Asp Gly Ala Ser Asn Gly Leu Ala Ala Pro 1825 1830 1835 1840 Asn Gly Pro Ser Gln Gln Arg Val Ile Asn Gln Ala Leu Ala Asn Ala 1845 1850 1855 Ala Leu Ser Ala Ser Asp Val Asp Ala Val Glu Ala His Gly Thr Gly 1860 1865 1870 Thr Arg Leu Gly Asp Pro Ile Glu Ala Gln Ala Leu Ile Ala Thr Tyr 1875 1880 1885 Gly Gln Ala Arg Glu Arg Asp Arg Pro Leu Trp Leu Gly Ser Val Lys 1890 1895 1900 Ser Asn Ile Gly His Thr Gln Ala Ala Ala Gly Val Ala Gly Val Ile 1905 1910 1915 1920 Lys Met Val Met Ala Met Arg His Gly Gln Leu Pro Ala Ser Leu His 1925 1930 1935 Ala Asp Glu Pro Thr Ser Glu Val Asp Trp Ser Ser Gly Ala Val Arg 1940 1945 1950 Leu Leu Ala Glu Gln Val Pro Trp Pro Glu Ser Asp Arg Val Arg Arg 1955 1960 1965 Val Gly Val Ser Ser Phe Gly Ile Ser Gly Thr Asn Ala His Val Ile 1970 1975 1980 Leu Glu Gln Ala Thr Asn Ala Pro Asp Ser Thr Ala Glu Thr Asp Lys 1985 1990 1995 2000 Thr Glu Ser Gly Ser Thr Val Asp Ile Pro Val Val Pro Trp Leu Val 2005 2010 2015 Ser Gly Lys Thr Thr Asp Ser Leu Arg Gly Gln Ala Glu Arg Val Leu 2020 2025 2030 Ser Gln Val Glu Ser Arg Pro Glu Gln Arg Ser Leu Asp Val Ala Tyr 2035 2040 2045 Ser Leu Ala Ser Gly Arg Ala Ala Leu Asp Glu Arg Ala Val Val Leu 2050 2055 2060 Gly Ala Asp Arg Gly Glu Leu Val Ala Gly Leu Ala Ala Leu Ala Ala 2065 2070 2075 2080 Gly Gln Glu Ala Ser Gly Val Ile Ser Gly Thr Arg Ala Ser Ala Arg 2085 2090 2095 Phe Gly Phe Val Phe Ser Gly Gln Gly Gly Gln Trp Leu Gly Met Gly 2100 2105 2110 Arg Ala Leu Tyr Ser Lys Phe Pro Val Phe Ala Ala Ala Phe Asp Glu 2115 2120 2125 Ala Cys Ala Glu Leu Glu Ala His Leu Gly Glu Asp Arg Arg Val Arg 2130 2135 2140 Asp Val Val Phe Gly Ser Asp Ala Gln Leu Leu Asp Gln Thr Leu Trp 2145 2150 2155 2160 Ala Gln Ser Gly Leu Phe Ala Leu Gln Ala Gly Leu Leu Gly Leu Leu 2165 2170 2175 Gly Ser Trp Gly Val Arg Pro Asp Val Val Met Gly His Ser Val Gly 2180 2185 2190 Glu Leu Ala Ala Ala Phe Ala Ala Gly Val Leu Ser Leu Arg Asp Ala 2195 2200 2205 Ala Arg Leu Val Ala Ala Arg Ala Arg Leu Met Gln Ala Leu Pro Ser 2210 2215 2220 Asp Gly Ala Met Leu Ala Val Ala Ala Gly Glu Asp Leu Val Arg Pro 2225 2230 2235 2240 Leu Leu Ala Gly Arg Glu Glu Ser Val Ser Val Ala Ala Leu Asn Ala 2245 2250 2255 Pro Gly Ser Val Val Leu Ser Gly Asp Arg Glu Val Leu Ala Ser Ile 2260 2265 2270 Val Gly Arg Leu Thr Glu Leu Arg Val Arg Thr Arg Arg Leu Arg Val 2275 2280 2285 Ser His Ala Phe His Ser His Arg Met Asp Pro Met Leu Gly Glu Phe 2290 2295 2300 Ala Gln Ile Ala Glu Ser Ala Glu Phe Gly Lys Pro Thr Thr Pro Leu 2305 2310 2315 2320 Val Ser Thr Leu Thr Gly Glu Leu Asp Arg Ala Ala Glu Met Ser Thr 2325 2330 2335 Pro Gly Tyr Trp Val Arg Gln Ala Arg Glu Pro Val Arg Phe Ala Asp 2340 2345 2350 Gly Val Gln Ala Leu Ala Ala Gln Gly Ile Gly Thr Val Val Glu Leu 2355 2360 2365 Gly Pro Asp Gly Thr Leu Ala Ala Leu Val Arg Glu Cys Ala Thr Glu 2370 2375 2380 Ser Asp Arg Val Gly Arg Ile Ser Ser Ile Pro Leu Met Arg Arg Glu 2385 2390 2395 2400 Arg Asp Glu Thr Arg Ser Val Met Thr Ala Leu Ala His Leu His Thr 2405 2410 2415 Arg Gly Gly Glu Val Asp Trp Gln Ala Phe Phe Ala Gly Thr Gly Ala 2420 2425 2430 Arg Gln Leu Glu Leu Pro Thr Tyr Ala Phe Gln Arg Gln His Tyr Trp 2435 2440 2445 Ile Glu Ser Ser Ala Arg Pro Ala Arg Asp Arg Ala Asp Ile Gly Glu 2450 2455 2460 Val Ala Glu Gln Phe Trp Thr Ala Val Asp Gln Gly Asp Leu Ala Thr 2465 2470 2475 2480 Leu Val Ala Ala Leu Asp Leu Gly Ala Asp Asp Asp Thr Cys Ala Ser 2485 2490 2495 Leu Ser Asp Val Leu Pro Ala Leu Ser Ser Trp Arg Ser Gly Leu Arg 2500 2505 2510 Asn Arg Ser Leu Val Asp Ser Cys Arg Tyr Arg Ile Ser Trp His Ser 2515 2520 2525 Ser Arg Glu Val Pro Ala Pro Lys Ile Ser Gly Thr Trp Leu Leu Val 2530 2535 2540 Val Pro Gly Ala Ala Asp Asp Gly Leu Val Thr Ala Leu Thr Ser Ser 2545 2550 2555 2560 Leu Val Gly Gly Gly Ala Glu Val Val Arg Ile Gly Leu Ser Glu Glu 2565 2570 2575 Asp Pro His Arg Glu Asp Val Ala Gln Arg Leu Ala Asn Ala Leu Thr 2580 2585 2590 Asp Ala Gly Gln Leu Gly Gly Val Leu Ser Leu Leu Gly Leu Asp Glu 2595 2600 2605 Ser Pro Ala Pro Gly Phe Ser Cys Leu Pro Thr Gly Phe Ala Leu Thr 2610 2615 2620 Val Gln Leu Leu Arg Ala Leu Arg Lys Ala Asp Val Glu Ala Pro Phe 2625 2630 2635 2640 Trp Ala Val Thr Arg Gly Gly Val Ala Leu Glu Asp Val Arg Val Ser 2645 2650 2655 Pro Glu Gln Ala Leu Val Trp Gly Leu Leu Arg Val Ala Gly Leu Glu 2660 2665 2670 His Pro Glu Phe Trp Gly Gly Leu Ile Asp Leu Pro Ser Asp Trp Asp 2675 2680 2685 Asp Arg Leu Gly Ala Arg Leu Ala Gly Val Leu Ala Asp Gly Gly Glu 2690 2695 2700 Asp Gln Val Ala Ile Arg Arg Gly Gly Val Phe Val Arg Arg Leu Glu 2705 2710 2715 2720 Arg Ala Gly Ala Ser Gly Ala Gly Ser Val Trp Arg Pro Arg Gly Thr 2725 2730 2735 Val Leu Val Thr Gly Gly Thr Gly Gly Leu Gly Ala His Val Ala Arg 2740 2745 2750 Trp Leu Ala Gly Ala Gly Ala Glu His Val Val Leu Thr Ser Arg Arg 2755 2760 2765 Gly Ala Asp Ala Pro Gly Ala Gly Glu Leu Arg Ala Glu Leu Glu Ala 2770 2775 2780 Leu Gly Ala Arg Val Ser Ile Val Pro Cys Asp Val Ala Asp Arg Asp 2785 2790 2795 2800 Ala Val Ala Gly Val Leu Ala Gly Ile Gly Gly Glu Cys Pro Leu Thr 2805 2810 2815 Ala Val Val His Ala Ala Gly Val Gly Glu Ala Gly Asp Val Val Glu 2820 2825 2830 Met Gly Leu Ala Asp Phe Ala Ala Val Leu Ser Ala Lys Val Arg Gly 2835 2840 2845 Ala Ala Asn Leu Asp Glu Leu Leu Ala Asp Ser Glu Leu Asp Ala Phe 2850 2855 2860 Val Met Phe Ser Ser Val Ser Gly Val Trp Gly Ala Gly Gly Gln Gly 2865 2870 2875 2880 Ala Tyr Ala Ala Ala Asn Ala Tyr Leu Asp Ala Leu Ala Glu Gln Arg 2885 2890 2895 Arg Ala Arg Gly Leu Val Gly Thr Ala Val Ala Trp Gly Pro Trp Ala 2900 2905 2910 Gly Asp Gly Met Ala Ala Gly Glu Thr Gly Ala Gln Leu His Arg Met 2915 2920 2925 Gly Leu Ala Ser Met Glu Pro Ser Ala Ala Leu Leu Ala Leu Gln Gly 2930 2935 2940 Ala Leu Asp Arg Asp Glu Thr Ser Leu Val Val Ala Asp Val Asp Trp 2945 2950 2955 2960 Ala Arg Phe Ala Pro Ala Phe Thr Ser Ala Arg Arg Arg Pro Leu Leu 2965 2970 2975 Asp Thr Ile Asp Glu Ala Arg Ala Ala Leu Glu Thr Thr Gly Glu Gln 2980 2985 2990 Ala Gly Thr Gly Lys Pro Val Glu Leu Thr Gln Arg Leu Ala Gly Leu 2995 3000 3005 Ser Arg Lys Glu Arg Asp Asp Ala Val Leu Asp Leu Val Arg Ala Glu 3010 3015 3020 Thr Ala Ala Val Leu Gly Arg Asp Asp Ala Thr Ala Leu Ala Pro Ser 3025 3030 3035 3040 Arg Pro Phe Gln Glu Leu Gly Phe Asp Ser Leu Met Ala Val Glu Leu 3045 3050 3055 Arg Asn Arg Leu Asn Thr Ala Thr Gly Ile Gln Leu Pro Ala Ser Thr 3060 3065 3070 Ile Phe Asp Tyr Pro Asn Ala Glu Ser Leu Ser Arg His Leu Cys Ala 3075 3080 3085 Glu Leu Phe Pro Thr Glu Thr Thr Val Asp Ser Ala Leu Ala Glu Leu 3090 3095 3100 Asp Arg Ile Glu Gln Gln Leu Ser Met Leu Thr Gly Glu Ala Arg Ala 3105 3110 3115 3120 Arg Asp Arg Ile Ala Thr Arg Leu Arg Ala Leu His Glu Lys Trp Asn 3125 3130 3135 Ser Ala Ala Glu Val Pro Thr Gly Ala Asp Val Leu Ser Thr Leu Asp 3140 3145 3150 Ser Ala Thr His Asp Glu Ile Phe Glu Phe Ile Asp Asn Glu Leu Asp 3155 3160 3165 Leu Ser 3170 5 4928 PRT Saccharopolyspora spinosa 5 Val Glu Ile Thr Met Ala Asn Glu Glu Lys Leu Phe Gly Tyr Leu Lys 1 5 10 15 Lys Val Thr Ala Asp Leu His Gln Thr Arg Gln Arg Leu Leu Ala Ala 20 25 30 Glu Ser Arg Ser Gln Glu Pro Ile Ala Ile Val Ser Ala Ser Cys Arg 35 40 45 Leu Pro Gly Gly Val Asp Ser Pro Glu Ala Leu Trp Gln Leu Val Arg 50 55 60 Thr Gly Thr Asp Ala Ile Ser Glu Phe Pro Ala Asp Arg Gly Trp Asp 65 70 75 80 Leu Gly Arg Leu Tyr Asp Pro Asp Pro Asn His Gln Gly Thr Ser Tyr 85 90 95 Thr Arg Ala Gly Gly Phe Leu Ala Gly Ala Gly Asp Phe Asp Pro Ala 100 105 110 Met Phe Gly Ile Ser Pro Arg Glu Ala Leu Ala Met Asp Pro Gln Gln 115 120 125 Arg Leu Leu Leu Glu Leu Ser Trp Glu Ala Leu Glu Arg Ala Gly Ile 130 135 140 Asp Pro Thr Ser Leu Arg Gly Ser Lys Thr Gly Val Phe Gly Gly Val 145 150 155 160 Thr Pro Gln Glu Tyr Gly Pro Ser Leu Gln Glu Met Ser Arg Asn Ala 165 170 175 Gly Gly Phe Gly Leu Thr Gly Arg Met Val Ser Val Ala Ser Gly Arg 180 185 190 Val Ala Tyr Ser Phe Gly Phe Glu Gly Pro Ala Val Thr Val Asp Thr 195 200 205 Ala Cys Ser Ser Ser Leu Val Ala Leu His Leu Ala Cys Gln Ser Leu 210 215 220 Arg Ser Gly Glu Cys Asp Leu Ala Leu Ala Gly Gly Val Thr Val Met 225 230 235 240 Ala Thr Pro Ala Thr Phe Val Glu Phe Ser Arg Gln Arg Gly Leu Ala 245 250 255 Pro Asp Gly Arg Cys Lys Ser Phe Ala Ala Ala Ala Asp Gly Thr Gly 260 265 270 Trp Gly Glu Gly Ala Gly Leu Val Leu Leu Glu Arg Leu Ser Asp Ala 275 280 285 Arg Arg Asn Gly His Glu Val Leu Ala Val Val Arg Gly Ser Ala Val 290 295 300 Asn Gln Asp Gly Ala Ser Asn Gly Leu Thr Ala Pro Asn Gly Pro Ser 305 310 315 320 Gln Gln Arg Val Ile Thr Gln Ala Leu Ala Ser Ala Gly Leu Ser Val 325 330 335 Ser Asp Val Asp Ala Val Glu Ala His Gly Thr Gly Thr Thr Leu Gly 340 345 350 Asp Pro Ile Glu Ala Gln Ala Leu Ile Ala Thr Tyr Gly Gln Gly Arg 355 360 365 Glu Lys Asp Arg Pro Leu Trp Leu Gly Ser Val Lys Ser Asn Ile Gly 370 375 380 His Thr Gln Ala Ala Ala Gly Val Ala Gly Val Ile Lys Met Val Leu 385 390 395 400 Ala Met Arg His Gly Gln Leu Pro Ala Thr Leu His Val Asp Glu Pro 405 410 415 Thr Ser Ala Val Asp Trp Ser Ala Gly Ser Val Arg Leu Leu Thr Glu 420 425 430 Asn Thr Pro Trp Pro Asp Ser Gly Arg Pro Cys Arg Val Gly Val Ser 435 440 445 Ser Phe Gly Ile Ser Gly Thr Asn Ala His Val Ile Leu Glu Gln Ser 450 455 460 Pro Val Glu Gln Gly Glu Pro Ala Gly Pro Val Glu Gly Glu Arg Glu 465 470 475 480 Pro Asp Val Ala Val Pro Val Val Pro Trp Val Leu Ser Gly Lys Thr 485 490 495 Pro Glu Ala Ala Arg Ala Gln Ala Glu Arg Val His Ser His Ile Glu 500 505 510 Asp Arg Pro Gly Leu Ser Pro Val Asp Val Ala Tyr Ser Leu Gly Met 515 520 525 Thr Arg Ala Ala Leu Asp Glu Arg Ala Val Val Leu Gly Ser Asp Arg 530 535 540 Ala Ala Leu Leu Thr Gly Leu Arg Ala Phe Ala Asp Gly Cys Asp Ala 545 550 555 560 Pro Glu Val Val Ser Gly Ser Val Gly Leu Gly Gly Arg Val Gly Phe 565 570 575 Val Phe Ser Gly Gln Gly Gly Gln Trp Pro Gly Met Gly Arg Gly Leu 580 585 590 Tyr Ser Val Phe Pro Val Phe Ala Asp Ala Phe Asp Glu Ala Cys Ala 595 600 605 Glu Leu Asp Ala His Leu Gly Gln Glu Leu Arg Val Arg Asp Val Val 610 615 620 Phe Gly Ser Gln Ala Trp Leu Leu Asp Arg Thr Val Trp Ala Gln Ser 625 630 635 640 Gly Leu Phe Ala Leu Gln Ile Gly Leu Leu Arg Leu Leu Gly Ser Trp 645 650 655 Gly Val Arg Pro Asp Val Val Leu Gly His Ser Val Gly Glu Leu Ala 660 665 670 Ala Val His Ala Ala Gly Val Leu Ser Leu Ser Glu Ala Ala Arg Leu 675 680 685 Val Ala Gly Arg Ala Arg Leu Met Gln Ala Leu Pro Ser Gly Gly Ala 690 695 700 Met Leu Ala Val Ala Thr Gly Glu Phe Gln Val Asp Pro Leu Leu Asp 705 710 715 720 Gly Val Arg Asp Arg Ile Gly Ile Ala Ala Val Asn Gly Pro Glu Ser 725 730 735 Val Val Leu Ser Gly Asp Arg Glu Leu Leu Thr Glu Ile Ala Asp Arg 740 745 750 Leu His Asp Gln Gly Cys Arg Thr Arg Trp Leu Arg Val Ser His Ala 755 760 765 Phe His Ser Pro His Met Glu Pro Met Leu Glu Glu Phe Ala Gln Ile 770 775 780 Ser Arg Gly Arg Glu Tyr His Ala Pro Glu Leu Pro Ile Ile Ser Thr 785 790 795 800 Leu Ile Gly Glu Leu Asp Gly Gly Arg Val Met Gly Thr Pro Glu Tyr 805 810 815 Trp Val Arg Gln Val Arg Glu Pro Val Arg Phe Ala Glu Gly Val Gln 820 825 830 Ala Leu Val Gly Gln Gly Val Gly Thr Ile Val Glu Leu Gly Pro Asp 835 840 845 Gly Ala Leu Ser Thr Leu Val Glu Glu Cys Val Ala Glu Ser Gly Arg 850 855 860 Val Ala Gly Ile Pro Leu Met Arg Lys Asp Arg Asp Glu Ala Arg Thr 865 870 875 880 Val Leu Ala Ala Leu Ala Gln Ile His Thr Arg Gly Gly Glu Val Asp 885 890 895 Trp Arg Ser Phe Phe Ala Gly Thr Gly Ala Lys Gln Val Asp Leu Pro 900 905 910 Thr Tyr Ala Phe Gln Arg Gln Arg Tyr Trp Leu Ala Ser Thr Gly Arg 915 920 925 Ala Gly Asp Val Thr Ala Ala Gly Leu Ala Glu Ala Asp His Pro Leu 930 935 940 Leu Gly Ala Val Val Ala Leu Ala Asp Gly Glu Gly Val Val Leu Thr 945 950 955 960 Gly Arg Leu Thr Ala Gly Ser His Pro Trp Leu Ser Asp His Arg Val 965 970 975 Leu Gly Glu Ile Val Val Pro Gly Thr Ala Ile Val Glu Leu Val Trp 980 985 990 His Val Gly Glu Arg Leu Gly Cys Gly Arg Val Glu Glu Leu Ala Leu 995 1000 1005 Glu Ala Pro Leu Ile Leu Pro Asp His Gly Ala Val Gln Val Gln Val 1010 1015 1020 Leu Val Gly Pro Pro Gly Glu Ser Gly Ala Arg Ser Val Ala Leu Tyr 1025 1030 1035 1040 Ser Cys Pro Gly Glu Ala Ile Glu Pro Glu Trp Lys Lys His Ala Thr 1045 1050 1055 Gly Val Leu Leu Pro Pro Val Ala Ala Glu Asn His Glu Leu Thr Ala 1060 1065 1070 Trp Pro Pro Glu Asn Ala Thr Glu Ile Asp Ala Asp Gly Val Tyr Ala 1075 1080 1085 Phe Leu Glu Gly His Gly Phe Ala Tyr Gly Pro Ala Phe Arg Cys Leu 1090 1095 1100 Arg Gly Ala Trp Arg Arg Gly Gly Glu Val Phe Ala Glu Val Ala Leu 1105 1110 1115 1120 Pro Asp Asp Met Gln Ala Gly Val Asp Arg Phe Gly Val His Pro Ala 1125 1130 1135 Leu Leu Asp Ala Val Leu His Ala Ala Ala Ala Glu Thr Ser Val Val 1140 1145 1150 Gln Ser Glu Ala Arg Val Pro Phe Ser Trp Arg Gly Val Glu Leu Arg 1155 1160 1165 Ala Thr Glu Ser Ala Val Val Arg Ala Arg Leu Ser Leu Thr Ser Asp 1170 1175 1180 Asp Glu Leu Ser Leu Val Ala Val Asp Pro Ala Gly Arg Phe Val Ala 1185 1190 1195 1200 Thr Val Asp Ser Leu Val Thr Arg Pro Ile Ser Arg Gln Gln Val Arg 1205 1210 1215 Ser Gly Ala Ile Gly Asp Cys Leu Phe Glu Val Glu Trp His Arg Lys 1220 1225 1230 Ala Leu Leu Gly Thr Thr Ala Gly Asp Asp Leu Ala Ile Val Gly Asp 1235 1240 1245 Gly Pro Ser Trp Pro Glu Ser Val Arg Ala Thr Ala Arg Phe Ala Thr 1250 1255 1260 Leu Asp Glu Phe Arg Ala Ala Val Asp Ser Asp Val Pro Ala Pro Gly 1265 1270 1275 1280 Ser Val Leu Val Ala Ala Met Ser Ala Glu Glu Val Glu Gly Gly Ser 1285 1290 1295 Leu Pro Ser Arg Ala Gln Glu Ser Thr Ser Asp Leu Leu Ala Leu Val 1300 1305 1310 Gln Ser Trp Leu Ala Asp Glu Arg Phe Ala Glu Ser Gln Leu Val Val 1315 1320 1325 Val Thr Arg Ala Ala Val Ser Ala Asp Ser Asp Ser Asp Val Ala Asp 1330 1335 1340 Leu Val Gly Ala Ser Ser Trp Gly Leu Leu Ser Ser Ala Gln Ser Glu 1345 1350 1355 1360 Asn Pro Gly Arg Phe Val Leu Val Asp Val Asp Gly Thr Pro Glu Ser 1365 1370 1375 Trp Gln Ala Leu Pro Ala Ala Val Arg Ala Gly Glu Pro Gln Leu Ala 1380 1385 1390 Leu Arg Arg Gly Val Ala Leu Val Pro Arg Leu Ala Arg Leu Thr Val 1395 1400 1405 Arg Glu Glu Gly Ser Ser Pro Gln Leu Asp Thr Asp Gly Thr Val Leu 1410 1415 1420 Ile Thr Gly Gly Thr Gly Ala Leu Gly Gly Val Val Ala Arg His Leu 1425 1430 1435 1440 Val Glu Glu His Gly Ile Arg Arg Leu Val Leu Ala Gly Arg Arg Gly 1445 1450 1455 Trp Asn Ala Pro Gly Val His Glu Leu Val Asp Glu Leu Ala Arg Ala 1460 1465 1470 Gly Ala Val Val Glu Val Val Ala Cys Asp Val Ala Asp Arg Thr Asp 1475 1480 1485 Leu Glu His Val Leu Ala Ala Ile Pro Val Asp Trp Pro Leu Arg Gly 1490 1495 1500 Ile Val His Thr Ala Gly Val Leu Ala Asp Gly Val Ile Gly Ser Leu 1505 1510 1515 1520 Ser Ala Ala Asp Val Gly Thr Val Phe Ala Pro Lys Val Thr Gly Ala 1525 1530 1535 Trp His Leu His Glu Leu Thr Arg Asp Leu Asp Leu Ser Phe Phe Val 1540 1545 1550 Leu Phe Ser Ser Phe Ser Gly Ile Ala Gly Ala Ala Gly Gln Ala Asn 1555 1560 1565 Tyr Ala Ala Ala Asn Thr Phe Leu Asp Ala Leu Ala Arg Tyr Arg Arg 1570 1575 1580 Ala Arg Gly Leu Pro Gly Leu Ser Leu Ala Trp Gly Leu Trp Ala Gln 1585 1590 1595 1600 Pro Ser Gly Met Thr Ser Gly Leu Asp Ala Ala Ser Val Glu Arg Leu 1605 1610 1615 Ala Arg Thr Gly Ile Ala Glu Leu Ser Thr Glu Asp Gly Leu Arg Leu 1620 1625 1630 Phe Asp Ala Ala Phe Ala Lys Asp Arg Ala Cys Val Val Ala Ala Arg 1635 1640 1645 Leu Asp Arg Ala Leu Leu Val Gly Asn Gly Arg Ser His Ala Ile Pro 1650 1655 1660 Ala Leu Leu Ser Ala Leu Val Pro Val Arg Gly Gly Val Ala Arg Lys 1665 1670 1675 1680 Thr Ala Asn Ser Gln Ala Ala Asp Glu Asp Ala Leu Leu Gly Leu Val 1685 1690 1695 Arg Glu His Val Ser Ala Val Leu Gly Tyr Ser Gly Ala Val Glu Val 1700 1705 1710 Gly Gly Asp Arg Ala Phe Arg Asp Leu Gly Phe Asp Ser Leu Ser Gly 1715 1720 1725 Val Glu Leu Arg Asn Arg Leu Ala Gly Val Leu Gly Val Arg Leu Pro 1730 1735 1740 Ala Thr Ala Val Phe Asp Tyr Pro Thr Pro Arg Ala Leu Ala Arg Phe 1745 1750 1755 1760 Leu His Gln Glu Leu Ala Gly Glu Val Ala Ser Thr Ser Thr Pro Val 1765 1770 1775 Thr Arg Ala Ala Ser Ala Glu Glu Asp Leu Val Ala Ile Val Gly Met 1780 1785 1790 Gly Cys Arg Phe Pro Gly Gly Val Ser Ser Pro Glu Glu Leu Trp Arg 1795 1800 1805 Leu Val Ala Gly Gly Val Asp Ala Val Ala Gly Phe Pro Asp Asp Arg 1810 1815 1820 Gly Trp Asp Leu Ala Ala Leu Tyr Asp Pro Asp Pro Asp Arg Leu Gly 1825 1830 1835 1840 Thr Ser Tyr Val Cys Glu Gly Gly Phe Leu Arg Asp Ala Ala Glu Phe 1845 1850 1855 Asp Ala Asp Met Phe Gly Ile Ser Pro Arg Glu Ala Leu Ala Met Asp 1860 1865 1870 Pro Gln Gln Arg Leu Leu Leu Glu Val Ala Trp Glu Thr Leu Glu Arg 1875 1880 1885 Ala Gly Ile Asp Pro Phe Ser Leu His Gly Ser Arg Thr Gly Val Phe 1890 1895 1900 Ala Gly Leu Met Tyr His Asp Tyr Gly Ala Arg Phe Ile Thr Arg Ala 1905 1910 1915 1920 Pro Glu Gly Phe Glu Gly His Leu Gly Thr Gly Asn Ala Gly Ser Val 1925 1930 1935 Leu Ser Gly Arg Val Ala Tyr Ser Phe Gly Phe Glu Gly Pro Ala Val 1940 1945 1950 Thr Val Asp Thr Ala Cys Ser Ser Ser Leu Val Ala Leu His Leu Ala 1955 1960 1965 Gly Gln Ala Leu Arg Ala Gly Glu Cys Glu Phe Ala Leu Ala Gly Gly 1970 1975 1980 Val Thr Val Met Ser Thr Pro Thr Thr Phe Val Glu Phe Ser Arg Gln 1985 1990 1995 2000 Arg Gly Leu Ala Pro Asp Gly Arg Cys Lys Ser Phe Ala Ala Ala Ala 2005 2010 2015 Asp Gly Thr Gly Trp Gly Glu Gly Ala Gly Leu Val Leu Leu Glu Arg 2020 2025 2030 Leu Ser Asp Ala Arg Arg Asn Gly His Glu Val Leu Ala Val Val Arg 2035 2040 2045 Gly Ser Ala Val Asn Gln Asp Gly Ala Ser Asn Gly Leu Thr Ala Pro 2050 2055 2060 Asn Gly Pro Ser Gln Gln Arg Val Ile Thr Gln Ala Leu Thr Ser Ala 2065 2070 2075 2080 Gly Leu Ser Val Ser Asp Val Asp Ala Val Glu Ala His Gly Thr Gly 2085 2090 2095 Thr Arg Leu Gly Asp Pro Ile Glu Ala Gln Ala Leu Ile Ala Thr Tyr 2100 2105 2110 Gly Arg Asp Arg Asp Pro Gly Arg Pro Leu Trp Leu Gly Ser Val Lys 2115 2120 2125 Ser Asn Ile Gly His Thr Gln Ala Ala Ala Gly Val Ala Gly Val Ile 2130 2135 2140 Lys Met Val Met Ala Met Arg Gln Gly Glu Leu Pro Arg Thr Leu His 2145 2150 2155 2160 Val Asp Glu Pro Ser Ala Gln Val Asp Trp Ser Ala Gly Thr Val Gln 2165 2170 2175 Leu Leu Thr Glu Asn Thr Pro Trp Pro Asp Ser Gly Arg Leu Arg Arg 2180 2185 2190 Ala Gly Val Ser Ser Phe Gly Ile Ser Gly Thr Asn Ala His Leu Ile 2195 2200 2205 Leu Glu Gln Pro Pro Arg Glu Ser Gln Arg Ser Thr Glu Pro Asp Ser 2210 2215 2220 Gly Ser Val Arg Asp Phe Pro Val Val Pro Trp Met Val Ser Gly Lys 2225 2230 2235 2240 Thr Pro Glu Ala Leu Ser Ala Gln Ala Asp Ala Leu Met Ser Tyr Leu 2245 2250 2255 Ser Asn Arg Val Asp Ala Ser Pro Arg Asp Ile Gly Tyr Ser Leu Ala 2260 2265 2270 Val Thr Arg Pro Ala Leu Asp His Arg Ala Val Val Leu Gly Ala Asp 2275 2280 2285 Arg Ala Ala Leu Leu Pro Gly Leu Lys Ala Leu Ala Val Ser Asn Asp 2290 2295 2300 Ala Ala Glu Val Ile Thr Gly Thr Arg Ala Ala Gly Pro Val Gly Phe 2305 2310 2315 2320 Val Phe Ser Gly Gln Gly Gly Gln Trp Pro Gly Met Gly Ser Gly Leu 2325 2330 2335 His Ser Ala Phe Pro Val Phe Ala Asp Ala Phe Asp Glu Ala Cys Cys 2340 2345 2350 Glu Leu Asp Ala His Leu Gly Gln Met Ala Arg Leu Arg Asp Val Leu 2355 2360 2365 Ser Gly Ser Asp Thr Gln Leu Leu Asp Gln Thr Leu Trp Ala Gln Pro 2370 2375 2380 Gly Leu Phe Ala Leu Gln Val Gly Leu Trp Glu Leu Leu Gly Ser Trp 2385 2390 2395 2400 Gly Val Arg Pro Ala Val Val Leu Gly His Ser Val Gly Glu Leu Ala 2405 2410 2415 Ala Ala Phe Ala Ala Gly Val Leu Ser Leu Arg Asp Ala Ala Arg Leu 2420 2425 2430 Val Ala Gly Arg Ala Arg Leu Met Gln Ala Leu Pro Thr Gly Gly Ala 2435 2440 2445 Met Leu Ala Ala Ala Ala Gly Glu Glu Gln Leu Arg Pro Leu Leu Ala 2450 2455 2460 Asp Cys Gly Asp Arg Val Gly Ile Ala Ala Val Asn Ala Pro Gly Ser 2465 2470 2475 2480 Val Val Leu Ser Gly Asp Arg Asp Val Leu Asp Asp Ile Ala Gly Arg 2485 2490 2495 Leu Asp Gly Gln Gly Ile Arg Ser Arg Trp Leu Arg Val Ser His Ala 2500 2505 2510 Phe His Ser His Arg Met Asp Pro Met Leu Ala Glu Phe Thr Glu Ile 2515 2520 2525 Ala Arg Ser Val Asp Tyr Arg Ser Ser Gly Leu Pro Ile Val Ser Thr 2530 2535 2540 Leu Thr Gly Glu Leu Asp Glu Val Gly Met Pro Ala Thr Pro Glu Tyr 2545 2550 2555 2560 Trp Val Arg Gln Val Arg Glu Pro Val Arg Phe Ala Asp Gly Val Ala 2565 2570 2575 Ala Leu Ala Ala His Gly Val Ser Thr Val Val Glu Val Gly Pro Asp 2580 2585 2590 Gly Val Leu Ser Ala Leu Val Gln Glu Cys Ala Ala Gly Ser Asp Gln 2595 2600 2605 Gly Gly Arg Val Ala Ala Val Pro Leu Met Arg Ser Asn Arg Asp Glu 2610 2615 2620 Ala His Thr Val Thr Thr Ala Leu Ala Gln Ile His Val Arg Gly Ala 2625 2630 2635 2640 Glu Val Asp Trp Arg Ser Phe Phe Ala Gly Thr Gly Ala Lys Gln Val 2645 2650 2655 Glu Leu Pro Thr Tyr Ala Phe Gln Arg Gln Arg Tyr Trp Leu Asp Ser 2660 2665 2670 Pro Ser Glu Pro Val Gly Gln Ser Ala Asp Pro Ala Arg Gln Ser Gly 2675 2680 2685 Phe Trp Glu Leu Val Glu Gln Glu Asp Val Ser Ala Leu Ser Ala Ala 2690 2695 2700 Leu His Ile Thr Gly Asp His Asp Val Gln Ala Ser Leu Glu Ser Val 2705 2710 2715 2720 Val Pro Val Leu Ser Ser Trp His Arg Arg Ile Arg Asn Glu Ser Leu 2725 2730 2735 Val His Gln Trp Arg Tyr Arg Ile Ser Trp His Glu Arg Ala Asp Leu 2740 2745 2750 Pro Asp Pro Ser Leu Ser Gly Thr Trp Leu Val Val Val Pro Glu Gly 2755 2760 2765 Trp Ser Ala Ser Arg Gln Val Leu Arg Phe Asn Glu Met Phe Glu Glu 2770 2775 2780 Arg Gly Cys Pro Ala Val Leu Phe Glu Leu Ala Gly His Asp Glu Glu 2785 2790 2795 2800 Ala Leu Ala Gln Arg Phe Arg Ser Leu Pro Val Ala Ser Gly Gly Ile 2805 2810 2815 Ser Gly Val Leu Ser Leu Leu Ala Leu Asp Glu Ser Pro Ser Ser Pro 2820 2825 2830 Asn Ala Ala Leu Pro Asn Gly Ala Leu Asn Ser Leu Val Leu Leu Arg 2835 2840 2845 Ala Leu Arg Ala Ala Asp Val Ser Ala Pro Leu Trp Leu Ala Thr Cys 2850 2855 2860 Gly Gly Val Ala Val Gly Asp Val Pro Val Asn Pro Gly Gln Ala Leu 2865 2870 2875 2880 Val Trp Gly Leu Gly Arg Val Val Gly Leu Glu His Pro Ala Trp Trp 2885 2890 2895 Gly Gly Leu Val Asp Val Pro Cys Leu Leu Asp Glu Asp Ala Arg Glu 2900 2905 2910 Arg Leu Ser Val Val Leu Ala Gly Leu Gly Glu Asp Glu Ile Ala Val 2915 2920 2925 Arg Pro Gly Gly Val Phe Val Arg Arg Leu Glu Arg Ala Gly Ala Ala 2930 2935 2940 Ser Gly Ala Gly Ser Val Trp Arg Pro Arg Gly Thr Val Leu Val Thr 2945 2950 2955 2960 Gly Gly Thr Gly Gly Leu Gly Ala His Val Ala Arg Trp Leu Ala Gly 2965 2970 2975 Ala Gly Ala Glu His Val Val Leu Thr Ser Arg Arg Gly Ala Ala Ala 2980 2985 2990 Pro Gly Ala Gly Asp Leu Arg Ala Glu Leu Glu Ala Leu Gly Ala Arg 2995 3000 3005 Val Ser Ile Thr Ala Cys Asp Val Ala Asp Arg Asp Ala Leu Ala Glu 3010 3015 3020 Val Leu Ala Thr Ile Pro Asp Asp Cys Pro Leu Thr Ala Val Met His 3025 3030 3035 3040 Ala Ala Gly Val Val Glu Val Gly Asp Val Ala Ser Met Cys Leu Thr 3045 3050 3055 Asp Phe Val Gly Val Leu Ser Ala Lys Ala Gly Gly Ala Ala Asn Leu 3060 3065 3070 Asp Glu Leu Leu Ala Asp Val Glu Leu Asp Ala Phe Val Leu Phe Ser 3075 3080 3085 Ser Val Ser Gly Val Trp Gly Ala Gly Gly Gln Gly Ala Tyr Ala Ala 3090 3095 3100 Ala Asn Ala Tyr Leu Asp Ala Leu Ala Gln Gln Arg Arg Ala Arg Gly 3105 3110 3115 3120 Leu Val Gly Thr Ala Val Ala Trp Gly Pro Trp Ala Gly Asp Gly Met 3125 3130 3135 Ala Ala Gly Glu Gly Gly Ala Gln Leu Arg Arg Ala Gly Leu Val Pro 3140 3145 3150 Met Ala Ala Asp Arg Ala Leu Leu Ala Leu Gln Gly Ala Leu Asp Arg 3155 3160 3165 Asp Glu Thr Ser Leu Val Val Ala Asp Met Ala Trp Glu Arg Phe Ala 3170 3175 3180 Pro Val Phe Ala Met Ser Arg Arg Arg Pro Leu Leu Asp Glu Leu Pro 3185 3190 3195 3200 Glu Ala Gln Gln Ala Leu Ala Asp Ala Glu Asn Thr Thr Asp Ala Ala 3205 3210 3215 Asp Ser Ala Val Pro Leu Pro Arg Leu Ala Gly Met Ala Ala Ala Glu 3220 3225 3230 Arg Arg Arg Ala Met Leu Asp Leu Val Leu Ala Glu Ala Ser Ile Val 3235 3240 3245 Leu Gly His Asn Gly Ser Asp Pro Val Gly Pro Asp Arg Ala Phe Gln 3250 3255 3260 Glu Leu Gly Phe Asp Ser Leu Met Ala Val Glu Leu Arg Asn Arg Leu 3265 3270 3275 3280 Gly Glu Ala Thr Gly Leu Ser Leu Pro Ala Thr Leu Ile Phe Asp Tyr 3285 3290 3295 Pro Ser Pro Ser Ala Leu Ala Glu Gln Leu Val Gly Glu Leu Val Gly 3300 3305 3310 Ala Gln Pro Ala Thr Thr Val Val Ala Gly Ala Asp Pro Val Asp Asp 3315 3320 3325 Pro Val Val Val Val Ala Met Gly Cys Arg Tyr Pro Gly Asp Val Cys 3330 3335 3340 Ser Pro Glu Glu Leu Trp Gln Leu Val Ser Ala Gly Arg Asp Ala Val 3345 3350 3355 3360 Ser Thr Phe Pro Val Asp Arg Gly Trp Asp Cys Asn Thr Leu Phe Asp 3365 3370 3375 Pro Asp Pro Asp Arg Ala Gly Ser Thr Tyr Val Arg Glu Gly Ala Phe 3380 3385 3390 Leu Thr Gly Ala Asp Arg Phe Asp Ala Gly Phe Phe Gly Ile Ser Pro 3395 3400 3405 Arg Glu Ala Arg Ala Met Asp Pro Gln Gln Arg Leu Leu Leu Glu Val 3410 3415 3420 Ala Trp Glu Val Phe Glu Arg Ala Gly Ile Ala Pro Leu Ser Leu Arg 3425 3430 3435 3440 Gly Ser Arg Thr Gly Val Phe Ala Gly Thr Asn Gly Gln Asp His Gly 3445 3450 3455 Ala Lys Val Ala Ala Ala Pro Glu Ala Ala Gly His Leu Leu Thr Gly 3460 3465 3470 Asn Ala Ala Ser Val Leu Ala Gly Arg Leu Ser Tyr Thr Phe Gly Leu 3475 3480 3485 Glu Gly Pro Ala Val Ala Val Asp Thr Ala Cys Ser Ser Ser Leu Val 3490 3495 3500 Ala Leu His Leu Ala Cys Gln Ser Leu Arg Ser Gly Glu Cys Asp Met 3505 3510 3515 3520 Ala Leu Ala Gly Gly Val Thr Val Met Ser Thr Pro Leu Ala Phe Leu 3525 3530 3535 Glu Phe Ser Arg Gln Arg Gly Leu Ala Pro Asp Gly Arg Cys Lys Ser 3540 3545 3550 Phe Ala Ala Ala Ala Asp Gly Thr Gly Trp Gly Glu Gly Ala Gly Leu 3555 3560 3565 Val Leu Leu Glu Arg Leu Ser Asp Ala Arg Arg Asn Gly His Arg Val 3570 3575 3580 Leu Ala Val Val Arg Gly Ser Ala Val Asn Gln Asp Gly Ala Ser Asn 3585 3590 3595 3600 Gly Leu Thr Ala Pro Asn Gly Pro Ser Gln Gln Arg Val Ile Arg Gln 3605 3610 3615 Ala Leu Ala Asn Ala Gly Leu Ser Ala Ser Asp Val Asp Val Val Glu 3620 3625 3630 Ala His Gly Thr Gly Thr Gly Leu Gly Asp Pro Ile Glu Ala Gln Ala 3635 3640 3645 Leu Ile Ala Thr Tyr Gly Gln Glu Arg Asp Pro Glu Arg Ala Leu Trp 3650 3655 3660 Leu Gly Ser Ile Lys Ser Asn Ile Gly His Thr Gln Ala Ala Ala Gly 3665 3670 3675 3680 Val Ala Gly Val Ile Lys Met Val Gln Ala Met Arg His Gly Glu Leu 3685 3690 3695 Pro Ala Thr Leu His Val Asp Lys Pro Thr Pro Gln Val Asp Trp Ser 3700 3705 3710 Ala Gly Ala Val Arg Leu Leu Thr Gly Asn Thr Pro Trp Pro Glu Ser 3715 3720 3725 Gly Arg Pro Arg Arg Ala Gly Val Ser Ser Phe Gly Ile Ser Gly Thr 3730 3735 3740 Asn Ala His Leu Ile Leu Glu Gln Pro Pro Ser Glu Pro Ala Glu Ile 3745 3750 3755 3760 Asp Gln Ser Asp Arg Arg Val Thr Ala His Pro Ala Val Ile Pro Trp 3765 3770 3775 Met Leu Ser Ala Arg Ser Leu Ala Ala Leu Gln Ala Gln Ala Ala Ala 3780 3785 3790 Leu Gln Ala Arg Leu Asp Arg Gly Pro Gly Ala Ser Pro Leu Asp Leu 3795 3800 3805 Gly Tyr Ser Leu Ala Thr Thr Arg Ser Val Leu Asp Glu Arg Ala Val 3810 3815 3820 Val Trp Gly Ala Asp Arg Glu Ala Leu Leu Ser Arg Leu Ala Ala Leu 3825 3830 3835 3840 Ala Asp Gly Arg Thr Ala Pro Gly Val Ile Thr Gly Ser Ala Asn Ser 3845 3850 3855 Gly Gly Arg Ile Gly Phe Val Phe Ser Gly Gln Gly Ser Gln Trp Leu 3860 3865 3870 Gly Met Gly Lys Ala Leu Cys Ala Ala Phe Pro Ala Phe Ala Asp Ala 3875 3880 3885 Phe Glu Glu Ala Cys Asp Ala Leu Ser Ala His Leu Gly Ala Asp Val 3890 3895 3900 Arg Gly Val Leu Phe Gly Ala Asp Glu Gln Met Leu Asp Arg Thr Leu 3905 3910 3915 3920 Trp Ala Gln Ser Gly Ile Phe Ala Val Gln Val Gly Leu Leu Gly Leu 3925 3930 3935 Leu Arg Ser Trp Gly Val Arg Pro Ala Ala Val Leu Gly His Ser Val 3940 3945 3950 Gly Glu Leu Ala Ala Ala His Ala Ala Gly Val Leu Ser Leu Pro Asp 3955 3960 3965 Ala Ala Arg Leu Val Ala Ala Arg Ala His Leu Met Gln Ala Leu Pro 3970 3975 3980 Thr Gly Gly Ala Met Leu Ala Val Ala Thr Ser Glu Ala Ala Val Gly 3985 3990 3995 4000 Pro Leu Leu Ser Gly Val Cys Asp Arg Val Ser Ile Ala Ala Ile Asn 4005 4010 4015 Gly Pro Glu Ser Val Val Leu Ser Gly Asp Arg Asp Val Leu Val Glu 4020 4025 4030 Leu Ala Gly Glu Phe Asp Ala Arg Gly Leu Arg Thr Lys Trp Leu Arg 4035 4040 4045 Val Ser His Ala Phe His Ser His Arg Met Glu Pro Ile Leu Asp Glu 4050 4055 4060 Tyr Ala Glu Thr Ala Arg Cys Val Glu Phe Gly Glu Pro Val Val Pro 4065 4070 4075 4080 Ile Val Ser Ala Ala Thr Gly Ala Leu Asp Thr Thr Gly Leu Met Cys 4085 4090 4095 Ala Ala Asp Tyr Trp Thr Arg Gln Val Arg Asp Pro Val Arg Phe Gly 4100 4105 4110 Asp Gly Val Arg Ala Leu Val Gly Gln Gly Val Asp Thr Ile Val Glu 4115 4120 4125 Phe Gly Pro Asp Gly Ala Leu Ser Ala Leu Val Glu Gln Cys Leu Ala 4130 4135 4140 Gly Ser Asp Gln Ala Gly Arg Val Ala Ala Ile Pro Leu Met Arg Arg 4145 4150 4155 4160 Asp Arg Asp Glu Val Glu Thr Ala Val Ala Ala Leu Ala His Val His 4165 4170 4175 Val Arg Gly Gly Ala Val Asp Trp Ser Ala Cys Phe Ala Gly Thr Gly 4180 4185 4190 Ala Arg Thr Val Glu Leu Pro Thr Tyr Ala Phe Gln Arg Gln Arg Tyr 4195 4200 4205 Trp Leu Ala Gly Gln Ala Asp Gly Arg Gly Gly Asp Val Val Ala Asp 4210 4215 4220 Pro Val Asp Ala Arg Phe Trp Glu Leu Val Glu Arg Ala Asp Pro Glu 4225 4230 4235 4240 Pro Leu Val Asp Glu Leu Cys Ile Asp Arg Asp Gln Pro Phe Arg Glu 4245 4250 4255 Val Leu Pro Val Leu Ala Ser Trp Arg Glu Lys Gln Arg Gln Glu Ala 4260 4265 4270 Leu Ala Asp Ser Trp Arg Tyr Gln Val Arg Trp Arg Ser Val Glu Val 4275 4280 4285 Pro Ser Ala Ala Ala Leu Arg Gly Val Trp Leu Val Val Leu Pro Ala 4290 4295 4300 Asp Val Pro Arg Asp Gln Pro Ala Val Val Ile Asp Ala Leu Ile Ala 4305 4310 4315 4320 Arg Gly Ala Glu Val Ala Val Leu Glu Leu Thr Glu Gln Asp Leu Gln 4325 4330 4335 Arg Ser Ala Leu Val Asp Lys Val Arg Ala Val Ile Ala Asp Arg Thr 4340 4345 4350 Glu Val Thr Gly Val Leu Ser Leu Leu Ala Met Asp Gly Met Pro Cys 4355 4360 4365 Ala Ala His Pro His Leu Ser Arg Gly Val Ala Ala Thr Val Ile Leu 4370 4375 4380 Thr Gln Val Leu Gly Asp Ala Gly Val Ser Ala Pro Leu Trp Leu Ala 4385 4390 4395 4400 Thr Thr Gly Gly Val Glu Ala Gly Thr Glu Asp Gly Pro Ala Asp Pro 4405 4410 4415 Asp His Gly Leu Ile Trp Gly Leu Gly Arg Val Val Gly Leu Glu His 4420 4425 4430 Pro Gln Trp Trp Gly Gly Leu Ile Asp Leu Pro Glu Thr Leu Asp Glu 4435 4440 4445 Thr Ser Arg Asn Gly Leu Val Ala Ala Leu Ala Gly Thr Ala Ala Glu 4450 4455 4460 Asp Gln Leu Ala Val Arg Ser Ser Gly Leu Phe Val Arg Arg Val Val 4465 4470 4475 4480 Arg Ala Ala Arg Asn Pro Arg Ser Glu Thr Trp Arg Ser Arg Gly Thr 4485 4490 4495 Val Leu Ile Thr Gly Gly Thr Gly Ala Leu Gly Ala Glu Val Ala Arg 4500 4505 4510 Trp Leu Ala Arg Arg Gly Ala Glu His Leu Val Leu Ile Ser Arg Arg 4515 4520 4525 Gly Pro Glu Ala Pro Gly Ala Ala Asp Leu Gly Ala Glu Leu Thr Glu 4530 4535 4540 Leu Gly Val Lys Val Thr Val Leu Ala Cys Asp Val Thr Asp Arg Asp 4545 4550 4555 4560 Glu Leu Ala Ala Val Leu Ala Ala Val Pro Thr Glu Tyr Pro Leu Ser 4565 4570 4575 Ala Val Val His Thr Ala Gly Val Gly Thr Pro Ala Asn Leu Ala Glu 4580 4585 4590 Thr Thr Leu Ala Gln Phe Ala Asp Val Leu Ser Ala Lys Val Val Gly 4595 4600 4605 Ala Ala Asn Leu Asp Arg Leu Leu Gly Gly Gln Pro Leu Asp Ala Phe 4610 4615 4620 Val Leu Phe Ser Ser Ile Ser Gly Val Trp Gly Ala Gly Gly Gln Gly 4625 4630 4635 4640 Ala Tyr Ser Ala Ala Asn Ala Tyr Leu Asp Ala Leu Ala Glu Arg Arg 4645 4650 4655 Arg Ala Cys Gly Arg Pro Ala Thr Cys Ile Ala Trp Gly Pro Trp Ala 4660 4665 4670 Gly Ala Gly Met Ala Val Gln Glu Gly Asn Glu Ala His Leu Arg Arg 4675 4680 4685 Arg Gly Leu Val Pro Met Glu Pro Gln Ser Ala Leu Phe Ala Leu Gln 4690 4695 4700 Gln Ala Leu Ser Gln Arg Glu Thr Ala Ile Thr Val Ala Asp Val Asp 4705 4710 4715 4720 Trp Glu Arg Phe Ala Ala Ser Phe Thr Ala Ala Arg Pro Arg Pro Leu 4725 4730 4735 Leu Glu Glu Ile Val Asp Leu Arg Pro Asp Thr Glu Thr Glu Glu Lys 4740 4745 4750 His Gly Ala Gly Glu Leu Gly Gln Gln Leu Ala Ala Leu Pro Pro Ala 4755 4760 4765 Glu Arg Gly His Leu Leu Leu Glu Val Val Leu Ala Glu Thr Ala Ser 4770 4775 4780 Thr Leu Gly His Asp Ser Ala Glu Ala Val Gln Pro Asp Arg Thr Phe 4785 4790 4795 4800 Ala Glu Leu Gly Phe Asp Ser Leu Thr Ala Val Glu Leu Arg Asn Arg 4805 4810 4815 Leu Asn Ala Val Thr Gly Leu Arg Leu Pro Pro Thr Leu Val Phe Asp 4820 4825 4830 His Pro Thr Pro Leu Ala Leu Ser Glu Gln Leu Val Pro Ala Leu Val 4835 4840 4845 Ala Glu Pro Asp Asn Gly Ile Glu Ser Leu Leu Ala Glu Leu Asp Arg 4850 4855 4860 Leu Asp Thr Thr Leu Ala Gln Gly Pro Ser Ile Pro Leu Glu Asp Gln 4865 4870 4875 4880 Ala Lys Val Ala Glu Arg Leu His Ala Leu Leu Ala Lys Trp Asp Gly 4885 4890 4895 Ala Arg Asp Gly Thr Ala Arg Ala Thr Ser Pro Gln Ser Leu Thr Ala 4900 4905 4910 Ala Thr Asp Asp Glu Ile Phe Asp Leu Ile Asp Arg Lys Phe Arg Arg 4915 4920 4925 6 5588 PRT Saccharopolyspora spinosa 6 Met Ala Asn Glu Glu Lys Leu Arg Glu Tyr Leu Lys Arg Val Val Val 1 5 10 15 Glu Leu Glu Glu Ala His Glu Arg Leu His Glu Leu Glu Arg Gln Glu 20 25 30 His Asp Pro Ile Ala Ile Val Ser Met Gly Cys Arg Tyr Pro Gly Gly 35 40 45 Val Ser Thr Pro Glu Glu Leu Trp Arg Leu Val Val Asp Gly Gly Asp 50 55 60 Ala Ile Ala Asn Phe Pro Glu Asp Arg Gly Trp Asn Leu Asp Glu Leu 65 70 75 80 Phe Asp Pro Asp Pro Gly Arg Ala Gly Thr Ser Tyr Val Arg Glu Gly 85 90 95 Gly Phe Leu Arg Gly Val Ala Asp Phe Asp Ala Gly Leu Phe Gly Ile 100 105 110 Ser Pro Arg Glu Ala Gln Ala Met Asp Pro Gln Gln Arg Leu Leu Leu 115 120 125 Glu Ile Ser Trp Glu Val Phe Glu Arg Ala Gly Ile Asp Pro Phe Ser 130 135 140 Leu Arg Gly Thr Lys Thr Gly Val Phe Ala Gly Leu Ile Tyr His Asp 145 150 155 160 Tyr Ala Ser Arg Phe Arg Lys Thr Pro Ala Glu Phe Glu Gly Tyr Phe 165 170 175 Ala Thr Gly Asn Ala Gly Ser Val Ala Ser Gly Arg Val Ala Tyr Thr 180 185 190 Phe Gly Leu Glu Gly Pro Ala Val Thr Val Asp Thr Ala Cys Ser Ser 195 200 205 Ser Leu Val Ala Leu His Leu Ala Cys Gln Ser Leu Arg Leu Gly Glu 210 215 220 Cys Asp Leu Ala Leu Ala Gly Gly Ile Ser Val Met Ala Thr Pro Gly 225 230 235 240 Ala Phe Val Glu Phe Ser Arg Gln Arg Ala Leu Ala Ser Asp Gly Arg 245 250 255 Cys Lys Pro Phe Ala Asp Ala Ala Asp Gly Thr Gly Trp Gly Glu Gly 260 265 270 Ala Gly Met Leu Leu Leu Glu Arg Leu Ser Asp Ala Arg Arg Asn Gly 275 280 285 His Pro Val Leu Ala Ala Val Val Gly Ser Ala Ile Asn Gln Asp Gly 290 295 300 Thr Ser Asn Gly Leu Thr Ala Pro Ser Gly Pro Ala Gln Gln Arg Val 305 310 315 320 Ile Arg Gln Ala Leu Ala Asn Ala Gly Leu Ser Pro Ala Glu Val Asp 325 330 335 Val Val Glu Ala His Gly Thr Gly Thr Ala Leu Gly Asp Pro Ile Glu 340 345 350 Ala Gln Ala Leu Ile Ala Thr Tyr Gly Ala Asn Arg Ser Ala Asp His 355 360 365 Pro Leu Leu Leu Gly Ser Leu Lys Ser Asn Ile Gly His Thr Gln Ala 370 375 380 Ala Ala Gly Val Ala Gly Val Ile Lys Ser Val Leu Ala Ile Arg His 385 390 395 400 Arg Glu Met Pro Arg Ser Leu His Ile Asp Gln Pro Ser Gln His Val 405 410 415 Asp Trp Ser Ala Gly Ala Val Arg Leu Leu Thr Asp Ser Val Asp Trp 420 425 430 Pro Asp Leu Gly Arg Pro Arg Arg Ala Gly Val Ser Ser Phe Gly Met 435 440 445 Ser Gly Thr Asn Ala His Leu Ile Val Glu Glu Val Ser Asp Glu Pro 450 455 460 Val Ser Gly Ser Thr Glu Pro Thr Gly Ala Phe Pro Trp Pro Leu Ser 465 470 475 480 Gly Lys Thr Glu Thr Ala Leu Arg Glu Gln Ala Ala Glu Leu Leu Ser 485 490 495 Val Val Thr Glu His Pro Glu Pro Gly Leu Gly Asp Val Gly Tyr Ser 500 505 510 Leu Ala Thr Gly Arg Ala Ala Met Glu His Arg Ala Val Val Val Ala 515 520 525 Asp Asp Arg Asp Ser Phe Val Ala Gly Leu Thr Ala Leu Ala Ala Gly 530 535 540 Val Pro Ala Ala Asn Val Val Gln Gly Ala Ala Asp Cys Lys Gly Lys 545 550 555 560 Val Ala Phe Val Phe Pro Gly Gln Gly Ser His Trp Gln Gly Met Ala 565 570 575 Arg Glu Leu Ser Glu Ser Ser Pro Val Phe Arg Arg Lys Leu Ala Glu 580 585 590 Cys Ala Ala Ala Thr Ala Pro Tyr Val Asp Trp Ser Leu Leu Gly Val 595 600 605 Leu Arg Gly Asp Pro Asp Ala Pro Ala Leu Asp Arg Asp Asp Val Ile 610 615 620 Gln Leu Ala Leu Phe Ala Met Met Val Ser Leu Ala Glu Leu Trp Arg 625 630 635 640 Ser Cys Gly Val Glu Pro Ala Ala Val Val Gly His Ser Gln Gly Glu 645 650 655 Ile Ala Ala Ala His Val Ala Gly Ala Leu Ser Leu Thr Asp Ala Val 660 665 670 Arg Ile Ile Ala Ala Arg Cys Asp Ala Val Ser Ala Leu Thr Gly Lys 675 680 685 Gly Gly Met Leu Ala Ile Ala Leu Pro Glu Ser Ala Val Val Lys Arg 690 695 700 Ile Ala Gly Leu Pro Glu Leu Thr Val Ala Ala Val Asn Gly Pro Gly 705 710 715 720 Ser Thr Val Val Ser Gly Glu Pro Ser Ala Leu Glu Arg Leu Gln Thr 725 730 735 Glu Leu Thr Ala Glu Asn Val Gln Thr Arg Arg Val Gly Ile Asp Tyr 740 745 750 Ala Ser His Ser Pro Gln Ile Ala Gln Val Gln Gly Arg Leu Leu Asp 755 760 765 Arg Leu Gly Glu Val Gly Ser Glu Pro Ala Glu Ile Ala Phe Tyr Ser 770 775 780 Thr Val Thr Gly Glu Arg Thr Asp Thr Gly Arg Leu Asp Ala Asp Tyr 785 790 795 800 Trp Tyr Gln Asn Leu Arg Gln Pro Val Arg Phe Gln Gln Thr Val Ala 805 810 815 Arg Met Ala Asp Gln Gly Tyr Arg Phe Phe Val Glu Val Ser Pro His 820 825 830 Pro Leu Leu Thr Ala Gly Ile Gln Glu Thr Leu Glu Ala Ala Asp Ala 835 840 845 Gly Gly Val Val Val Gly Ser Leu Arg Arg Gly Glu Gly Gly Ser Arg 850 855 860 Arg Trp Leu Thr Ser Leu Ala Glu Cys Gln Val Arg Gly Leu Pro Val 865 870 875 880 Asn Trp Glu Gln Val Phe Leu Asn Thr Gly Ala Arg Arg Val Pro Leu 885 890 895 Pro Thr Tyr Pro Phe Gln Arg Gln Arg Tyr Trp Leu Glu Ser Ala Glu 900 905 910 Tyr Asp Ala Gly Asp Leu Gly Ser Val Gly Leu Leu Ser Ala Glu His 915 920 925 Pro Leu Leu Gly Ala Ala Val Thr Leu Ala Asp Ala Gly Gly Phe Leu 930 935 940 Leu Thr Gly Lys Leu Ser Val Lys Thr Gln Pro Trp Leu Ala Asp His 945 950 955 960 Val Val Gly Gly Ala Ile Leu Leu Pro Gly Thr Ala Phe Val Glu Met 965 970 975 Leu Ile Arg Ala Ala Asp Gln Val Gly Cys Asp Leu Ile Glu Glu Leu 980 985 990 Ser Leu Thr Thr Pro Leu Val Leu Pro Ala Thr Gly Ala Val Gln Val 995 1000 1005 Gln Ile Ala Val Gly Gly Pro Asp Glu Ala Gly Arg Arg Ser Val Arg 1010 1015 1020 Val His Ser Cys Arg Asp Asp Ala Val Pro Gln Asp Ser Trp Thr Cys 1025 1030 1035 1040 His Ala Thr Gly Thr Leu Thr Ser Ser Asp His Gln Asp Ala Gly Gln 1045 1050 1055 Gly Pro Asp Gly Ile Trp Pro Pro Asn Asp Ala Val Ala Val Pro Leu 1060 1065 1070 Asp Ser Phe Tyr Ala Arg Ala Ala Glu Arg Gly Phe Asp Phe Gly Pro 1075 1080 1085 Ala Phe Gln Gly Leu Gln Ala Ala Trp Lys Arg Gly Asp Glu Ile Phe 1090 1095 1100 Ala Glu Val Gly Leu Pro Thr Ala His Arg Glu Asp Ala Gly Arg Phe 1105 1110 1115 1120 Gly Ile His Pro Ala Leu Leu Asp Ala Ala Leu Gln Ala Leu Gly Ala 1125 1130 1135 Ala Glu Glu Asp Pro Asp Glu Gly Trp Leu Pro Phe Ala Trp Gln Gly 1140 1145 1150 Val Ser Leu Lys Ala Thr Gly Ala Leu Ser Leu Arg Val His Leu Val 1155 1160 1165 Pro Ala Gly Ala Asn Ala Val Ser Val Phe Thr Thr Asp Thr Thr Gly 1170 1175 1180 Gln Ala Val Leu Ser Ile Asp Ser Leu Val Leu Arg Gln Ile Ser Asp 1185 1190 1195 1200 Lys Gln Leu Ala Ala Ala Arg Ala Met Glu His Glu Ser Leu Phe Arg 1205 1210 1215 Val Asp Trp Lys Arg Ile Ser Pro Gly Ala Ala Lys Pro Val Ser Trp 1220 1225 1230 Ala Val Ile Gly Asn Asp Glu Leu Ala Arg Ala Cys Gly Ser Ala Leu 1235 1240 1245 Gly Thr Glu Leu His Pro Asp Leu Thr Gly Leu Ala Asp Pro Pro Pro 1250 1255 1260 Asp Val Val Val Val Pro Cys Gly Ala Ser Arg Gln Asp Leu Asp Val 1265 1270 1275 1280 Ala Ser Glu Ala Arg Ala Ala Thr Gln Arg Met Leu Asp Leu Ile Gln 1285 1290 1295 Asp Trp Leu Ala Ala Ala Arg Phe Ala Gly Ser Arg Leu Val Val Val 1300 1305 1310 Thr Cys Gly Ala Ala Ser Thr Gly Pro Ala Glu Gly Val Ser Asp Leu 1315 1320 1325 Val His Ala Ala Ser Trp Gly Leu Leu Arg Ser Ala Gln Ser Glu Asn 1330 1335 1340 Pro Asp Arg Phe Val Leu Val Asp Val Asp Gly Thr Ala Glu Ser Trp 1345 1350 1355 1360 Arg Ala Leu Ala Ala Ala Val Arg Ser Gly Glu Pro Gln Leu Ala Leu 1365 1370 1375 Arg Ala Gly Glu Val Arg Val Pro Arg Leu Ala Arg Cys Val Ala Ala 1380 1385 1390 Glu Asp Ser Arg Ile Pro Val Pro Gly Ala Asp Gly Thr Val Leu Ile 1395 1400 1405 Ser Gly Gly Thr Gly Leu Leu Gly Gly Leu Val Ala Arg His Leu Val 1410 1415 1420 Ala Glu Arg Gly Val Arg Arg Leu Val Leu Ala Gly Arg Arg Gly Trp 1425 1430 1435 1440 Ser Ala Pro Gly Val Thr Asp Leu Val Asp Glu Leu Val Gly Leu Gly 1445 1450 1455 Ala Ala Val Glu Val Ala Ser Cys Asp Val Gly Asp Arg Ala Gln Leu 1460 1465 1470 Asp Arg Leu Leu Thr Thr Ile Ser Ala Glu Phe Pro Leu Arg Gly Val 1475 1480 1485 Val His Ala Ala Gly Ala Leu Ala Asp Gly Val Val Glu Ser Leu Thr 1490 1495 1500 Pro Glu His Val Ala Lys Val Phe Gly Pro Lys Ala Ala Gly Ala Trp 1505 1510 1515 1520 His Leu His Glu Leu Thr Leu Asp Leu Asp Leu Ser Phe Phe Val Leu 1525 1530 1535 Phe Ser Ser Phe Ser Gly Val Ala Gly Ala Ala Gly Gln Gly Asn Tyr 1540 1545 1550 Ala Ala Ala Asn Ala Phe Leu Asp Gly Leu Ala Gln His Arg Arg Thr 1555 1560 1565 Ala Gly Leu Pro Ala Val Ser Leu Ala Trp Gly Leu Trp Glu Gln Pro 1570 1575 1580 Ser Gly Met Thr Gly Ala Leu Asp Ala Ala Gly Arg Ser Arg Ile Ala 1585 1590 1595 1600 Arg Thr Asn Pro Pro Met Ser Ala Pro Asp Gly Leu Arg Leu Phe Glu 1605 1610 1615 Met Ala Phe Arg Val Pro Gly Glu Ser Leu Leu Val Pro Val His Val 1620 1625 1630 Asp Leu Asn Ala Leu Arg Ala Asp Ala Ala Asp Gly Gly Val Pro Ala 1635 1640 1645 Leu Leu Arg Asp Leu Val Pro Ala Pro Val Arg Arg Ser Ala Val Asn 1650 1655 1660 Glu Ser Ala Asp Val Asn Gly Leu Val Gly Arg Leu Arg Arg Leu Pro 1665 1670 1675 1680 Asp Leu Asp Gln Glu Thr Gln Leu Leu Gly Leu Val Arg Glu His Val 1685 1690 1695 Ser Ala Val Leu Gly His Ser Gly Ala Val Glu Val Gly Ala Asp Arg 1700 1705 1710 Ala Phe Arg Asp Leu Gly Phe Asp Ser Leu Ser Gly Val Glu Phe Arg 1715 1720 1725 Asn Arg Leu Gly Gly Val Leu Gly Val Arg Leu Pro Ala Thr Ala Val 1730 1735 1740 Phe Asp Tyr Pro Thr Pro Arg Ala Leu Val Arg Phe Leu Leu Asp Lys 1745 1750 1755 1760 Leu Ile Gly Gly Val Glu Ala Pro Thr Pro Ala Pro Ala Ala Val Ala 1765 1770 1775 Ala Val Thr Ala Asp Asp Pro Val Val Ile Val Gly Met Gly Cys Arg 1780 1785 1790 Tyr Pro Gly Gly Val Ser Ser Pro Glu Glu Leu Trp Arg Leu Val Ala 1795 1800 1805 Gly Gly Leu Asp Ala Val Ala Glu Phe Pro Asp Asp Arg Gly Trp Asp 1810 1815 1820 Gln Ala Gly Leu Phe Asp Pro Asp Pro Asp Arg Leu Gly Thr Ser Tyr 1825 1830 1835 1840 Val Cys Glu Gly Gly Phe Leu Arg Asp Ala Ala Glu Phe Asp Ala Gly 1845 1850 1855 Phe Phe Gly Ile Ser Pro Arg Glu Ala Leu Ala Met Asp Pro Gln Gln 1860 1865 1870 Arg Leu Leu Leu Glu Val Ala Trp Glu Thr Val Glu Arg Ala Gly Ile 1875 1880 1885 Asp Pro Leu Ser Leu Arg Gly Ser Arg Thr Gly Val Phe Ala Gly Leu 1890 1895 1900 Met His His Asp Tyr Gly Ala Arg Phe Ile Thr Arg Ala Pro Glu Gly 1905 1910 1915 1920 Phe Glu Gly Tyr Leu Gly Asn Gly Ser Ala Gly Gly Val Phe Ser Gly 1925 1930 1935 Arg Val Ala Tyr Ser Phe Gly Phe Glu Gly Pro Ala Val Thr Val Asp 1940 1945 1950 Thr Ala Cys Ser Ser Ser Leu Val Ala Leu His Leu Ala Gly Gln Ala 1955 1960 1965 Leu Arg Ser Gly Glu Cys Asp Leu Ala Leu Ala Gly Gly Val Thr Val 1970 1975 1980 Met Ala Thr Pro Gly Met Phe Val Glu Phe Ser Arg Gln Arg Gly Leu 1985 1990 1995 2000 Ala Ala Asp Gly Arg Cys Lys Ser Phe Ala Ala Ala Ala Asp Gly Thr 2005 2010 2015 Gly Trp Gly Glu Gly Ala Gly Leu Val Leu Leu Glu Arg Leu Ser Asp 2020 2025 2030 Ala Arg Arg Asn Gly His Ala Val Leu Ala Val Val Arg Gly Ser Ala 2035 2040 2045 Val Asn Gln Asp Gly Ala Ser Asn Gly Leu Thr Ala Pro Asn Gly Pro 2050 2055 2060 Ser Gln Gln Arg Val Ile Thr Gln Ala Leu Ala Ser Ala Gly Leu Ser 2065 2070 2075 2080 Val Ser Asp Val Asp Ala Val Glu Ala His Gly Thr Gly Thr Arg Leu 2085 2090 2095 Gly Asp Pro Ile Glu Ala Gln Ala Leu Ile Ala Thr Tyr Gly Gln Gly 2100 2105 2110 Arg Asp Ser Asp Arg Pro Leu Trp Leu Gly Ser Val Lys Ser Asn Ile 2115 2120 2125 Gly His Thr Gln Ala Ala Ala Gly Val Ala Gly Val Ile Lys Met Val 2130 2135 2140 Met Ala Met Arg His Gly Gln Leu Pro Ala Thr Leu His Val Asp Glu 2145 2150 2155 2160 Pro Thr Ser Glu Val Asp Trp Ser Ala Gly Asp Val Gln Leu Leu Thr 2165 2170 2175 Glu Asn Thr Pro Trp Pro Gly Asn Ser His Pro Arg Arg Val Gly Val 2180 2185 2190 Ser Ser Phe Gly Ile Ser Gly Thr Asn Ala His Val Ile Leu Glu Gln 2195 2200 2205 Ala Ser Lys Thr Pro Asp Glu Thr Ala Asp Lys Ser Gly Pro Asp Ser 2210 2215 2220 Glu Ser Thr Val Asp Leu Pro Ala Val Pro Leu Ile Val Ser Gly Arg 2225 2230 2235 2240 Thr Pro Ala Ala Leu Ser Ala Gln Ala Ser Ala Leu Leu Ser Tyr Leu 2245 2250 2255 Gly Glu Arg Gly Asp Ile Ser Thr Leu Asp Ala Ala Phe Ser Leu Ala 2260 2265 2270 Ser Ser Arg Ala Ala Leu Glu Glu Arg Ala Val Val Leu Gly Ala Asp 2275 2280 2285 Arg Glu Thr Leu Leu Ser Gly Leu Glu Ala Leu Ala Ser Gly Arg Glu 2290 2295 2300 Ala Ser Gly Val Val Ser Gly Ser Pro Val Ser Gly Gly Val Gly Phe 2305 2310 2315 2320 Val Phe Ala Gly Gln Gly Gly Gln Trp Leu Gly Met Gly Arg Gly Leu 2325 2330 2335 Tyr Ser Val Phe Pro Val Phe Ala Asp Ala Phe Asp Glu Ala Cys Ala 2340 2345 2350 Gly Leu Asp Ala His Leu Gly Gln Asp Val Gly Val Arg Asp Val Val 2355 2360 2365 Phe Gly Ser Asp Gly Ser Leu Leu Asp Arg Thr Leu Trp Ala Gln Ser 2370 2375 2380 Gly Leu Phe Ala Leu Gln Val Gly Leu Leu Ser Leu Leu Gly Ser Trp 2385 2390 2395 2400 Gly Val Arg Pro Gly Val Val Leu Gly His Ser Val Gly Glu Phe Ala 2405 2410 2415 Ala Ala Val Ala Ala Gly Val Leu Ser Leu Pro Asp Ala Ala Arg Met 2420 2425 2430 Val Ala Gly Arg Ala Arg Leu Met Gln Ala Leu Pro Ser Gly Gly Ala 2435 2440 2445 Met Leu Ala Val Ala Ala Gly Glu Glu Gln Leu Arg Pro Leu Leu Ala 2450 2455 2460 Asp Arg Val Asp Gly Ala Gly Ile Ala Ala Val Asn Ala Pro Glu Ser 2465 2470 2475 2480 Val Val Leu Ser Gly Asp Arg Glu Val Leu Asp Asp Ile Ala Gly Ala 2485 2490 2495 Leu Asp Gly Gln Gly Ile Arg Trp Arg Arg Leu Arg Val Ser His Ala 2500 2505 2510 Phe His Ser Tyr Arg Met Asp Pro Met Leu Gln Glu Phe Ala Glu Ile 2515 2520 2525 Ala Arg Ser Val Asp Tyr Arg Arg Gly Asp Leu Pro Val Val Ser Thr 2530 2535 2540 Leu Thr Gly Glu Leu Asp Thr Ala Gly Val Met Ala Thr Pro Glu Tyr 2545 2550 2555 2560 Trp Val Arg Gln Val Arg Glu Pro Val Arg Phe Ala Asp Gly Val Arg 2565 2570 2575 Val Leu Ala Gln Gln Gly Val Ala Thr Ile Phe Glu Leu Gly Pro Asp 2580 2585 2590 Ala Thr Leu Ser Ala Leu Ile Pro Asp Cys His Ser Trp Ala Asp Gln 2595 2600 2605 Ala Met Pro Ile Pro Met Leu Arg Lys Asp Arg Thr Glu Thr Glu Thr 2610 2615 2620 Val Val Ala Ala Val Ala Arg Ala His Thr Arg Gly Val Pro Val Glu 2625 2630 2635 2640 Trp Ser Ala Tyr Phe Ala Gly Thr Gly Ala Arg Arg Val Glu Leu Pro 2645 2650 2655 Thr Tyr Ala Phe Gln Arg Gln Arg Tyr Trp Leu Glu Thr Ser Asp Tyr 2660 2665 2670 Gly Asp Val Thr Gly Ile Gly Leu Ala Ala Ala Glu His Pro Leu Leu 2675 2680 2685 Gly Ala Val Val Ala Leu Ala Asp Gly Asp Gly Met Val Leu Thr Gly 2690 2695 2700 Arg Leu Ser Val Gly Thr His Pro Trp Leu Ala Gln His Arg Val Leu 2705 2710 2715 2720 Gly Glu Val Val Val Pro Gly Thr Ala Ile Leu Glu Met Ala Leu His 2725 2730 2735 Ala Gly Ala Arg Leu Gly Cys Asp Arg Val Glu Glu Leu Thr Leu Glu 2740 2745 2750 Thr Pro Leu Val Val Pro Glu Arg Ala Ala Gly Ala Gly Ser Arg Gly 2755 2760 2765 Pro Ala Gly Gly Thr Thr Val Ser Ile Glu Thr Ala Glu Glu Arg Val 2770 2775 2780 Arg Thr Asn Asp Ala Ile Glu Ile Gln Leu Leu Val Asn Ala Pro Asp 2785 2790 2795 2800 Glu Gly Gly Arg Arg Arg Val Ser Leu Tyr Ser Arg Pro Ala Gly Gly 2805 2810 2815 Ser Arg Gly Gly Gly Trp Thr Arg His Ala Thr Gly Glu Leu Val Val 2820 2825 2830 Gly Thr Thr Gly Gly Arg Ala Val Pro Asp Trp Ser Ala Glu Gly Ala 2835 2840 2845 Glu Ser Ile Ala Leu Asp Glu Phe Tyr Val Ala Leu Ala Gly Asn Gly 2850 2855 2860 Phe Glu Tyr Gly Pro Leu Phe Gln Gly Leu Gln Ala Ala Trp Arg Arg 2865 2870 2875 2880 Gly Asp Glu Val Leu Ala Glu Ile Ala Pro Pro Ala Glu Ala Asp Ala 2885 2890 2895 Met Ala Ser Gly Tyr Leu Leu Asp Pro Ala Leu Leu Asp Ala Ala Leu 2900 2905 2910 Gln Ala Ser Ala Leu Gly Asp Arg Pro Glu Gln Gly Gly Ala Trp Leu 2915 2920 2925 Pro Phe Ser Phe Thr Gly Val Glu Leu Ser Ala Pro Ala Gly Thr Ile 2930 2935 2940 Ser Arg Val Arg Leu Glu Thr Arg Arg Pro Asp Ala Ile Ser Val Ala 2945 2950 2955 2960 Val Met Asp Glu Ser Gly Arg Leu Leu Ala Ser Ile Asp Ser Leu Arg 2965 2970 2975 Leu Arg Ser Val Ser Ser Gly Gln Leu Ala Asn Arg Asp Ala Val Arg 2980 2985 2990 Asp Ala Leu Phe Glu Val Thr Trp Glu Pro Val Ala Thr Gln Ser Thr 2995 3000 3005 Glu Pro Gly Arg Trp Ala Leu Leu Gly Asp Thr Ala Cys Gly Lys Asp 3010 3015 3020 Asp Leu Ile Lys Leu Ala Thr Asp Ser Ala Asp Arg Cys Ala Asp Leu 3025 3030 3035 3040 Ala Ala Leu Ala Glu Lys Leu Asp Ser Ser Ala Leu Val Pro Asp Val 3045 3050 3055 Val Val Tyr Cys Ala Gly Glu Gln Ala Asp Pro Gly Thr Gly Ala Ala 3060 3065 3070 Ala Leu Ala Glu Thr Gln Gln Thr Leu Ala Leu Leu Gln Ala Trp Leu 3075 3080 3085 Ala Glu Pro Arg Leu Ala Glu Ala Arg Leu Val Val Val Thr Cys Ala 3090 3095 3100 Ala Val Thr Thr Ala Pro Ser Asp Gly Ala Ser Glu Leu Ala His Ala 3105 3110 3115 3120 Pro Leu Trp Gly Leu Leu Arg Ala Ala Gln Val Glu Asn Pro Gly Gln 3125 3130 3135 Phe Val Leu Ala Asp Val Asp Gly Thr Ala Glu Ser Trp Arg Ala Leu 3140 3145 3150 Pro Ser Ala Leu Gly Ser Met Glu Pro Gln Leu Ala Leu Arg Lys Gly 3155 3160 3165 Ala Val Arg Ala Pro Arg Leu Ala Ser Val Ala Gly Gln Ile Asp Val 3170 3175 3180 Pro Ala Val Val Ala Asp Pro Asp Arg Thr Val Leu Ile Ser Gly Gly 3185 3190 3195 3200 Thr Gly Leu Leu Gly Gly Ala Val Ala Arg His Leu Val Thr Glu Arg 3205 3210 3215 Gly Val Arg Arg Leu Val Leu Thr Gly Arg Arg Gly Trp Asp Ala Pro 3220 3225 3230 Gly Ile Thr Glu Leu Val Gly Glu Leu Asn Gly Leu Gly Ala Val Val 3235 3240 3245 Asp Val Val Ala Cys Asp Val Ala Asp Arg Ala Asp Leu Glu Ser Leu 3250 3255 3260 Leu Ala Ala Val Pro Ala Glu Phe Pro Leu Cys Gly Val Val His Ala 3265 3270 3275 3280 Ala Gly Ala Leu Ala Asp Gly Val Ile Glu Ser Leu Ser Pro Asp Asp 3285 3290 3295 Val Gly Ala Val Phe Gly Pro Lys Ala Ala Gly Ala Trp Asn Leu His 3300 3305 3310 Glu Leu Thr Arg Asp Thr Asp Leu Ser Phe Phe Ala Leu Phe Ser Ser 3315 3320 3325 Leu Ser Gly Val Ala Gly Ala Pro Gly Gln Gly Asn Tyr Ala Ala Ala 3330 3335 3340 Asn Ala Phe Leu Asp Ala Leu Ala His Tyr Arg Arg Ser Gln Gly Leu 3345 3350 3355 3360 Pro Ala Val Ser Leu Ala Trp Gly Leu Trp Glu Gln Pro Ser Gly Met 3365 3370 3375 Thr Glu Thr Leu Ser Glu Val Asp Arg Ser Arg Ile Ala Arg Ala Asn 3380 3385 3390 Pro Pro Leu Ser Thr Lys Glu Gly Leu Arg Leu Phe Asp Ala Gly Leu 3395 3400 3405 Ala Leu Asp Arg Ala Ala Val Val Pro Ala Lys Leu Asp Arg Thr Phe 3410 3415 3420 Leu Ala Glu Gln Ala Arg Ser Gly Ser Leu Pro Ala Leu Leu Thr Ala 3425 3430 3435 3440 Leu Val Pro Pro Ile Arg Arg Asn Arg Arg Ala Ser Gly Thr Glu Leu 3445 3450 3455 Ala Asp Glu Gly Thr Leu Leu Gly Val Val Arg Glu His Ala Ala Ala 3460 3465 3470 Val Leu Gly Tyr Ser Ser Ala Ala Asp Val Gly Val Glu Arg Ala Phe 3475 3480 3485 Arg Asp Leu Gly Phe Asp Ser Leu Ser Gly Val Glu Leu Arg Asn Arg 3490 3495 3500 Leu Ala Gly Val Leu Gly Val Arg Leu Pro Ala Thr Ala Val Phe Asp 3505 3510 3515 3520 Tyr Pro Thr Pro Arg Ala Leu Ala Arg Phe Leu His Gln Glu Leu Ala 3525 3530 3535 Asp Glu Ile Ala Thr Thr Pro Ala Pro Val Thr Thr Thr Arg Ala Pro 3540 3545 3550 Val Ala Glu Asp Asp Leu Val Ala Ile Val Gly Met Gly Cys Arg Phe 3555 3560 3565 Pro Gly Gln Val Ser Ser Pro Glu Glu Leu Trp Arg Leu Val Ala Gly 3570 3575 3580 Gly Val Asp Ala Val Ala Asp Phe Pro Ala Asp Arg Gly Trp Asp Leu 3585 3590 3595 3600 Ala Gly Leu Phe Asp Pro Asp Pro Glu Arg Ala Gly Lys Thr Tyr Val 3605 3610 3615 Arg Glu Gly Ala Phe Leu Thr Asp Ala Asp Arg Phe Asp Ala Gly Phe 3620 3625 3630 Phe Gly Ile Ser Pro Arg Glu Ala Leu Ala Met Asp Pro Gln Gln Arg 3635 3640 3645 Leu Leu Leu Glu Leu Ser Trp Glu Ala Ile Glu Arg Ala Gly Ile Asp 3650 3655 3660 Pro Gly Ser Leu Arg Gly Ser Arg Thr Gly Val Phe Ala Gly Leu Met 3665 3670 3675 3680 Tyr His Asp Tyr Gly Ala Arg Phe Ala Ser Arg Ala Pro Glu Gly Phe 3685 3690 3695 Glu Gly Tyr Leu Gly Asn Gly Ser Ala Gly Ser Val Ala Ser Gly Arg 3700 3705 3710 Ile Ala Tyr Ser Phe Gly Phe Glu Gly Pro Ala Val Thr Val Asp Thr 3715 3720 3725 Ala Cys Ser Ser Ser Leu Val Ala Leu His Leu Ala Gly Gln Ser Leu 3730 3735 3740 Arg Ser Gly Glu Cys Asp Leu Ala Leu Ala Gly Gly Val Thr Val Met 3745 3750 3755 3760 Ser Thr Pro Gly Thr Phe Val Glu Phe Ser Arg Gln Arg Gly Leu Ala 3765 3770 3775 Pro Asp Gly Arg Cys Lys Ser Phe Ala Glu Ser Ala Asp Gly Thr Gly 3780 3785 3790 Trp Gly Glu Gly Ala Gly Leu Val Leu Leu Glu Arg Leu Ser Asp Ala 3795 3800 3805 Arg Arg Asn Gly His Arg Val Leu Ala Val Val Arg Gly Ser Ala Val 3810 3815 3820 Asn Gln Asp Gly Ala Ser Asn Gly Leu Thr Ala Pro Asn Gly Pro Ser 3825 3830 3835 3840 Gln Gln Arg Val Ile Gln Gln Ala Leu Ala Ser Ala Gly Leu Ser Val 3845 3850 3855 Ser Asp Val Asp Ala Val Glu Ala His Gly Thr Gly Thr Arg Leu Gly 3860 3865 3870 Asp Pro Ile Glu Ala Gln Ala Leu Ile Ala Thr Tyr Gly Arg Asp Arg 3875 3880 3885 Asp Pro Gly Arg Pro Leu Trp Leu Gly Ser Val Lys Ser Asn Ile Gly 3890 3895 3900 His Thr Gln Ala Ala Ala Gly Val Ala Gly Val Ile Lys Met Val Met 3905 3910 3915 3920 Ala Met Arg His Gly Gln Leu Pro Arg Thr Leu His Val Asp Ala Pro 3925 3930 3935 Ser Ser Gln Val Asp Trp Ser Ala Gly Arg Val Gln Leu Leu Thr Glu 3940 3945 3950 Asn Thr Pro Trp Pro Asp Ser Gly Arg Pro Cys Arg Val Gly Val Ser 3955 3960 3965 Ser Phe Gly Ile Ser Gly Thr Asn Ala His Val Ile Leu Glu Gln Ser 3970 3975 3980 Thr Gly Gln Met Asp Gln Ala Ala Glu Pro Asp Ser Ser Pro Val Leu 3985 3990 3995 4000 Asp Val Pro Val Val Pro Trp Val Val Ser Gly Lys Thr Pro Glu Ala 4005 4010 4015 Leu Ser Ala Gln Ala Ala Thr Leu Ala Thr Tyr Leu Asp Gln Asn Val 4020 4025 4030 Asp Val Ser Pro Leu Asp Val Gly Ile Ser Leu Ala Val Thr Arg Ser 4035 4040 4045 Ala Leu Asp Glu Arg Ala Val Val Leu Gly Ser Asp Arg Asp Thr Leu 4050 4055 4060 Leu Ser Gly Leu Asn Ala Leu Ala Ala Gly His Glu Ala Ala Gly Val 4065 4070 4075 4080 Val Thr Gly Pro Val Gly Ile Gly Gly Arg Thr Gly Phe Val Phe Ala 4085 4090 4095 Gly Gln Gly Gly Gln Trp Leu Gly Met Gly Arg Arg Leu Tyr Ser Glu 4100 4105 4110 Phe Pro Ala Phe Ala Gly Ala Phe Asp Glu Ala Cys Ala Glu Leu Asp 4115 4120 4125 Ala Asn Leu Gly Arg Glu Val Gly Val Arg Asp Val Val Phe Gly Ser 4130 4135 4140 Asp Glu Ser Leu Leu Asp Arg Thr Leu Trp Ala Gln Ser Gly Leu Phe 4145 4150 4155 4160 Ala Leu Gln Val Gly Leu Trp Glu Leu Leu Gly Thr Trp Gly Val Arg 4165 4170 4175 Pro Ser Val Val Leu Gly His Ser Val Gly Glu Leu Ala Ala Ala Phe 4180 4185 4190 Ala Ala Gly Val Leu Ser Met Ala Glu Ala Ala Arg Leu Val Ala Gly 4195 4200 4205 Arg Ala Arg Leu Met Gln Ala Leu Pro Ser Gly Gly Ala Met Leu Ala 4210 4215 4220 Val Ser Ala Thr Glu Ala Arg Val Gly Pro Leu Leu Asp Gly Val Arg 4225 4230 4235 4240 Asp Arg Val Gly Val Ala Ala Val Asn Ala Pro Gly Ser Val Val Leu 4245 4250 4255 Ser Gly Asp Arg Asp Val Leu Asp Gly Ile Ala Gly Arg Leu Asp Gly 4260 4265 4270 Gln Gly Ile Arg Ser Arg Trp Leu Arg Val Ser His Ala Phe His Ser 4275 4280 4285 His Arg Met Asp Pro Met Leu Ala Glu Phe Ala Glu Leu Ala Arg Ser 4290 4295 4300 Val Asp Tyr Arg Ser Pro Arg Leu Pro Ile Val Ser Thr Leu Thr Gly 4305 4310 4315 4320 Asn Leu Asp Asp Val Gly Val Met Ala Thr Pro Glu Tyr Trp Val Arg 4325 4330 4335 Gln Val Arg Glu Pro Val Arg Phe Ala Asp Gly Val Gln Ala Leu Val 4340 4345 4350 Asp Gln Gly Val Asp Thr Ile Val Glu Leu Gly Pro Asp Gly Ala Leu 4355 4360 4365 Ser Ser Leu Val Gln Glu Cys Val Ala Glu Ser Gly Arg Ala Thr Gly 4370 4375 4380 Ile Pro Leu Val Arg Arg Asp Arg Asp Glu Val Arg Thr Val Leu Asp 4385 4390 4395 4400 Ala Leu Ala Gln Thr His Thr Arg Gly Gly Ala Val Asp Trp Gly Ser 4405 4410 4415 Phe Phe Ala Gly Thr Arg Ala Thr Gln Val Asp Leu Pro Thr Tyr Ala 4420 4425 4430 Phe Gln Arg Gln Arg Tyr Trp Leu Glu Pro Ser Asp Ser Gly Asp Val 4435 4440 4445 Thr Gly Val Gly Leu Thr Gly Ala Glu His Pro Leu Leu Gly Ala Val 4450 4455 4460 Val Pro Val Ala Gly Gly Asp Glu Val Leu Leu Thr Gly Arg Leu Ser 4465 4470 4475 4480 Val Gly Thr His Pro Trp Leu Ala Glu His Arg Val Leu Gly Glu Val 4485 4490 4495 Val Val Pro Gly Thr Ala Leu Leu Glu Met Ala Trp Arg Ala Gly Ser 4500 4505 4510 Gln Val Gly Cys Glu Arg Val Glu Glu Leu Thr Leu Glu Ala Pro Leu 4515 4520 4525 Val Leu Pro Glu Arg Gly Ala Ala Ala Val Gln Leu Ala Val Gly Ala 4530 4535 4540 Pro Asp Glu Ala Gly Arg Arg Ser Leu Gln Leu Tyr Ser Arg Gly Ala 4545 4550 4555 4560 Asp Glu Asp Gly Asp Trp Arg Arg Ile Ala Ser Gly Leu Leu Ala Gln 4565 4570 4575 Ala Asn Ala Val Pro Pro Ala Asp Ser Thr Ala Trp Pro Pro Asp Gly 4580 4585 4590 Ala Gly Gln Val Asp Leu Ala Glu Phe Tyr Glu Arg Leu Ala Glu Arg 4595 4600 4605 Gly Leu Thr Tyr Gly Pro Val Phe Gln Gly Leu Arg Ala Ala Trp Arg 4610 4615 4620 His Gly Asp Asp Ile Phe Ala Glu Leu Ala Gly Ser Pro Asp Ala Ser 4625 4630 4635 4640 Gly Phe Gly Ile His Pro Ala Leu Leu Asp Ala Ala Leu His Ala Met 4645 4650 4655 Ala Leu Gly Ala Ser Pro Asp Ser Glu Ala Arg Leu Pro Phe Ser Trp 4660 4665 4670 Arg Gly Ala Gln Leu Tyr Arg Ala Glu Gly Ala Ala Leu Arg Val Arg 4675 4680 4685 Leu Ser Pro Leu Gly Ser Gly Ala Val Ser Leu Thr Leu Val Asp Ala 4690 4695 4700 Thr Gly Arg Arg Val Ala Ala Val Glu Ser Leu Ser Thr Arg Pro Val 4705 4710 4715 4720 Ser Thr Asp Gln Ile Gly Ala Gly Arg Gly Asp Gln Glu Arg Leu Leu 4725 4730 4735 His Val Glu Trp Val Arg Ser Ala Glu Ser Ala Gly Met Ser Leu Thr 4740 4745 4750 Ser Cys Ala Val Val Gly Leu Gly Glu Pro Glu Trp His Ala Ala Leu 4755 4760 4765 Lys Thr Thr Gly Val Gln Val Glu Ser His Ala Asp Leu Ala Ser Leu 4770 4775 4780 Ala Thr Glu Val Ala Lys Arg Gly Ser Ala Pro Gly Ala Val Ile Val 4785 4790 4795 4800 Pro Cys Pro Arg Pro Arg Ala Met Gln Glu Leu Pro Thr Ala Ala Arg 4805 4810 4815 Arg Ala Thr Gln Gln Ala Met Ala Met Leu Gln Gln Trp Leu Ala Asp 4820 4825 4830 Asp Arg Phe Val Ser Thr Arg Leu Ile Leu Leu Thr His Arg Ala Val 4835 4840 4845 Ser Ala Val Ala Gly Glu Asp Val Leu Asp Leu Val His Ala Pro Leu 4850 4855 4860 Trp Gly Leu Val Arg Ser Ala Gln Ala Glu His Pro Asp Arg Phe Ala 4865 4870 4875 4880 Leu Ile Asp Met Asp Asp Glu Arg Ala Ser Gln Thr Ala Leu Ala Glu 4885 4890 4895 Ala Leu Thr Ala Gly Glu Ala Gln Leu Ala Val Arg Ser Gly Val Val 4900 4905 4910 Leu Ala Pro Arg Leu Gly Gln Val Lys Val Ser Gly Gly Glu Ala Phe 4915 4920 4925 Arg Trp Asp Glu Gly Thr Val Leu Val Thr Gly Gly Thr Gly Gly Leu 4930 4935 4940 Gly Ala Leu Leu Ala Arg His Leu Val Ser Ala His Gly Val Arg His 4945 4950 4955 4960 Leu Leu Leu Ala Ser Arg Arg Gly Leu Ala Ala Pro Gly Ala Asp Glu 4965 4970 4975 Leu Val Ala Glu Leu Glu Gln Ala Gly Ala Asp Val Ala Val Val Ala 4980 4985 4990 Cys Asp Ser Ala Asp Arg Asp Ser Leu Ala Arg Leu Val Ala Ser Val 4995 5000 5005 Pro Ala Glu Asn Pro Leu Arg Val Val Val His Ala Ala Gly Val Leu 5010 5015 5020 Asp Asp Gly Val Leu Met Ser Met Ser Pro Glu Arg Leu Asp Ala Val 5025 5030 5035 5040 Leu Arg Pro Lys Val Asp Ala Ala Trp Tyr Leu His Glu Leu Thr Arg 5045 5050 5055 Glu Leu Gly Leu Ser Ala Phe Val Leu Phe Ser Ser Val Ala Gly Leu 5060 5065 5070 Phe Gly Gly Ala Gly Gln Ser Asn Tyr Ala Ala Gly Asn Ala Phe Leu 5075 5080 5085 Asp Ala Leu Ala His Cys Arg Gln Ala Gln Gly Leu Pro Ala Leu Ser 5090 5095 5100 Leu Ala Ser Gly Leu Trp Ala Ser Ile Asp Gly Met Ala Gly Asp Leu 5105 5110 5115 5120 Ala Ala Ala Asp Val Glu Arg Leu Ser Arg Ala Gly Ile Gly Pro Leu 5125 5130 5135 Ser Ala Pro Gly Gly Leu Ala Leu Phe Asp Ala Ala Val Gly Ser Asp 5140 5145 5150 Glu Pro Leu Leu Ala Pro Val Arg Leu Asp Val Glu Ala Leu Arg Val 5155 5160 5165 Gln Ala Arg Ser Val Gln Thr Arg Ile Pro Glu Met Leu His Gly Met 5170 5175 5180 Ala Met Gly Pro Ser Arg Arg Thr Pro Phe Thr Ser Arg Val Glu Pro 5185 5190 5195 5200 Leu His Glu Arg Leu Ala Gly Leu Ser Glu Gly Glu Arg Arg Gln Gln 5205 5210 5215 Val Leu Gln Arg Val Arg Ala Asp Ile Ala Val Val Leu Gly His Gly 5220 5225 5230 Arg Ser Ser Asp Val Asp Ile Glu Lys Pro Leu Ala Glu Leu Gly Phe 5235 5240 5245 Asp Ser Leu Thr Ala Ile Glu Leu Arg Asn Arg Leu Ala Thr Ala Thr 5250 5255 5260 Gly Leu Arg Leu Pro Ala Thr Leu Ala Phe Asp His Gly Thr Ala Ala 5265 5270 5275 5280 Ala Leu Ala Gln His Val Cys Ala Gln Leu Gly Thr Ala Thr Ala Pro 5285 5290 5295 Ala Pro Arg Arg Thr Asp Asp Asn Asp Ala Thr Glu Pro Val Arg Ser 5300 5305 5310 Leu Phe Gln Gln Ala Tyr Ala Ala Gly Arg Ile Leu Asp Gly Met Asp 5315 5320 5325 Leu Val Lys Val Ala Ala Gln Leu Arg Pro Val Phe Gly Ser Pro Gly 5330 5335 5340 Glu Leu Glu Ser Leu Pro Lys Pro Val Gln Leu Ser Arg Gly Pro Glu 5345 5350 5355 5360 Glu Leu Ala Leu Val Cys Met Pro Ala Leu Ile Gly Met Pro Pro Ala 5365 5370 5375 Gln Gln Tyr Ala Arg Ile Ala Ala Gly Phe Arg Asp Val Arg Asp Val 5380 5385 5390 Ser Val Ile Pro Met Pro Gly Phe Ile Ala Gly Glu Pro Leu Pro Ser 5395 5400 5405 Ala Ile Glu Val Ala Val Arg Thr Gln Ala Glu Ala Val Leu Gln Glu 5410 5415 5420 Phe Ala Gly Gly Ser Phe Val Leu Val Gly His Ser Ser Gly Gly Trp 5425 5430 5435 5440 Leu Ala His Glu Val Ala Gly Glu Leu Glu Arg Arg Gly Val Val Pro 5445 5450 5455 Ala Gly Val Val Leu Leu Asp Thr Tyr Ile Pro Gly Glu Ile Thr Pro 5460 5465 5470 Arg Phe Ser Val Ala Met Ala His Arg Thr Tyr Glu Lys Leu Ala Thr 5475 5480 5485 Phe Thr Asp Met Gln Asp Val Gly Ile Thr Ala Met Gly Gly Tyr Phe 5490 5495 5500 Arg Met Phe Thr Glu Trp Thr Pro Thr Pro Ile Gly Ala Pro Thr Leu 5505 5510 5515 5520 Phe Val Arg Thr Glu Asp Cys Val Ala Asp Pro Glu Gly Arg Pro Trp 5525 5530 5535 Thr Asp Asp Ser Trp Arg Pro Gly Trp Thr Leu Ala Asp Ala Thr Val 5540 5545 5550 Gln Val Pro Gly Asp His Phe Ser Met Met Asp Glu His Ala Gly Ser 5555 5560 5565 Thr Ala Gln Ala Val Ala Ser Trp Leu Asp Lys Leu Asn Gln Arg Thr 5570 5575 5580 Ala Arg Gln Arg 5585 7 275 PRT Saccharopolyspora spinosa 7 Val Leu Pro Gly Gly Ala Pro Thr Ser Gln Gln Val Gly Gln Met Tyr 1 5 10 15 Asp Leu Val Thr Pro Leu Leu Asn Ser Val Ala Gly Gly Pro Cys Ala 20 25 30 Ile His His Gly Tyr Trp Glu Asn Asp Gly Arg Ala Ser Trp Gln Gln 35 40 45 Ala Ala Asp Arg Leu Thr Asp Leu Val Ala Glu Arg Thr Val Leu Asp 50 55 60 Gly Gly Val Arg Leu Leu Asp Val Gly Cys Gly Thr Gly Gln Pro Ala 65 70 75 80 Leu Arg Val Ala Arg Asp Asn Ala Ile Gln Ile Thr Gly Ile Thr Val 85 90 95 Ser Gln Val Gln Val Ala Ile Ala Ala Asp Cys Ala Arg Glu Arg Gly 100 105 110 Leu Ser His Arg Val Asp Phe Ser Cys Val Asp Ala Met Ser Leu Pro 115 120 125 Tyr Pro Asp Asn Ala Phe Asp Ala Ala Trp Ala Met Gln Ser Leu Leu 130 135 140 Glu Met Ser Glu Pro Asp Arg Ala Ile Arg Glu Ile Leu Arg Val Leu 145 150 155 160 Lys Pro Gly Gly Ile Leu Gly Val Thr Glu Val Val Lys Arg Glu Ala 165 170 175 Gly Gly Gly Met Pro Val Ser Gly Asp Arg Trp Pro Thr Gly Leu Arg 180 185 190 Ile Cys Leu Ala Glu Gln Leu Leu Glu Ser Leu Arg Ala Ala Gly Phe 195 200 205 Glu Ile Leu Asp Trp Glu Asp Val Ser Ser Arg Thr Arg Tyr Phe Met 210 215 220 Pro Gln Phe Ala Glu Glu Leu Ala Ala His Gln His Gly Ile Ala Asp 225 230 235 240 Arg Tyr Gly Pro Ala Val Ala Gly Trp Ala Ala Ala Val Cys Asp Tyr 245 250 255 Glu Lys Tyr Ala His Asp Met Gly Tyr Ala Ile Leu Thr Ala Arg Lys 260 265 270 Pro Val Gly 275 8 390 PRT Saccharopolyspora spinosa 8 Met Arg Val Leu Val Val Pro Leu Pro Tyr Pro Thr His Leu Met Ala 1 5 10 15 Met Val Pro Leu Cys Trp Ala Leu Gln Ala Ser Gly His Glu Val Leu 20 25 30 Ile Ala Ala Pro Pro Glu Leu Gln Ala Thr Ala His Gly Ala Gly Leu 35 40 45 Thr Thr Ala Gly Ile Arg Gly Asn Asp Arg Thr Gly Asp Thr Gly Gly 50 55 60 Thr Thr Gln Leu Arg Phe Pro Asn Pro Ala Phe Gly Gln Arg Asp Thr 65 70 75 80 Glu Ala Gly Arg Gln Leu Trp Glu Gln Thr Ala Ser Asn Val Ala Gln 85 90 95 Ser Ser Leu Asp Gln Leu Pro Glu Tyr Leu Arg Leu Ala Glu Ala Trp 100 105 110 Arg Pro Ser Val Leu Leu Val Asp Val Cys Ala Leu Ile Gly Arg Val 115 120 125 Leu Gly Gly Leu Leu Asp Leu Pro Val Val Leu His Arg Trp Gly Val 130 135 140 Asp Pro Thr Ala Gly Pro Phe Ser Asp Arg Ala His Glu Leu Leu Asp 145 150 155 160 Pro Val Cys Arg His His Gly Leu Thr Gly Leu Pro Thr Pro Glu Leu 165 170 175 Ile Leu Asp Pro Cys Pro Pro Ser Leu Gln Ala Ser Asp Ala Pro Gln 180 185 190 Gly Ala Pro Val Gln Tyr Val Pro Tyr Asn Gly Ser Gly Ala Phe Pro 195 200 205 Ala Trp Gly Ala Ala Arg Thr Ser Ala Arg Arg Val Cys Ile Cys Met 210 215 220 Gly Arg Met Val Leu Asn Ala Thr Gly Pro Ala Pro Leu Leu Arg Ala 225 230 235 240 Val Ala Ala Ala Thr Glu Leu Pro Gly Val Glu Ala Val Ile Ala Val 245 250 255 Pro Pro Glu His Arg Ala Leu Leu Thr Asp Leu Pro Asp Asn Ala Arg 260 265 270 Ile Ala Glu Ser Val Pro Leu Asn Leu Phe Leu Arg Thr Cys Glu Leu 275 280 285 Val Ile Cys Ala Gly Gly Ser Gly Thr Ala Phe Thr Ala Thr Arg Leu 290 295 300 Gly Ile Pro Gln Leu Val Leu Pro Gln Tyr Phe Asp Gln Phe Asp Tyr 305 310 315 320 Ala Arg Asn Leu Ala Ala Ala Gly Ala Gly Ile Cys Leu Pro Asp Glu 325 330 335 Gln Ala Gln Ser Asp His Glu Gln Phe Thr Asp Ser Ile Ala Thr Val 340 345 350 Leu Gly Asp Thr Gly Phe Ala Ser Ala Ala Ile Lys Leu Ser Asp Glu 355 360 365 Ile Thr Ala Met Pro His Pro Ala Ala Leu Val Arg Thr Leu Glu Asn 370 375 380 Thr Ala Ala Ile Arg Ala 385 390 9 250 PRT Saccharopolyspora spinosa 9 Met Pro Ser Gln Asn Ala Leu Tyr Leu Asp Leu Leu Lys Lys Val Leu 1 5 10 15 Thr Asn Thr Ile Tyr Ser Asp Arg Pro His Pro Asn Ala Trp Gln Asp 20 25 30 Asn Thr Asp Tyr Arg Gln Ala Ala Arg Ala Lys Gly Thr Asp Trp Pro 35 40 45 Thr Val Ala His Thr Met Ile Gly Leu Glu Arg Leu Asp Asn Leu Gln 50 55 60 His Cys Val Glu Ala Val Leu Ala Asp Gly Val Pro Gly Asp Phe Ala 65 70 75 80 Glu Thr Gly Val Trp Arg Gly Gly Ala Cys Ile Phe Met Arg Ala Val 85 90 95 Leu Gln Ala Phe Gly Asp Thr Gly Arg Thr Val Trp Val Val Asp Ser 100 105 110 Phe Gln Gly Met Pro Glu Ser Ser Ala Gln Asp His Gln Ala Asp Gln 115 120 125 Ala Met Ala Leu His Glu Tyr Asn Asp Val Leu Gly Val Ser Leu Glu 130 135 140 Thr Val Arg Gln Asn Phe Ala Arg Tyr Gly Leu Leu Asp Glu Gln Val 145 150 155 160 Arg Phe Leu Pro Gly Trp Phe Arg Asp Thr Leu Pro Thr Ala Pro Ile 165 170 175 Gln Glu Leu Ala Val Leu Arg Leu Asp Gly Asp Leu Tyr Glu Ser Thr 180 185 190 Met Asp Ser Leu Arg Asn Leu Tyr Pro Lys Leu Ser Pro Gly Gly Phe 195 200 205 Val Ile Ile Asp Asp Tyr Phe Leu Pro Ser Cys Gln Asp Ala Val Lys 210 215 220 Gly Phe Arg Ala Glu Leu Gly Ile Thr Glu Pro Ile His Asp Ile Asp 225 230 235 240 Gly Thr Gly Ala Tyr Trp Arg Arg Ser Trp 245 250 10 395 PRT Saccharopolyspora spinosa 10 Met Ser Glu Ile Ala Val Ala Pro Trp Ser Val Val Glu Arg Leu Leu 1 5 10 15 Leu Ala Ala Gly Ala Gly Pro Ala Lys Leu Gln Glu Ala Val Gln Val 20 25 30 Ala Gly Leu Asp Ala Val Ala Asp Ala Ile Val Asp Glu Leu Val Val 35 40 45 Arg Cys Asp Pro Leu Ser Leu Asp Glu Ser Val Arg Ile Gly Leu Glu 50 55 60 Ile Thr Ser Gly Ala Gln Leu Val Arg Arg Thr Val Glu Leu Asp His 65 70 75 80 Ala Gly Leu Arg Leu Ala Ala Val Ala Glu Ala Ala Ala Val Leu Arg 85 90 95 Phe Asp Ala Val Asp Leu Leu Glu Gly Leu Phe Gly Pro Val Asp Gly 100 105 110 Arg Arg His Asn Ser Arg Glu Val Arg Trp Ser Asp Ser Met Thr Gln 115 120 125 Phe Ser Pro Asp Gln Gly Leu Ala Gly Ala Gln Arg Leu Leu Ala Phe 130 135 140 Arg Asn Arg Val Ser Thr Ala Val His Ala Val Leu Ala Ala Ala Ala 145 150 155 160 Thr Arg Arg Ala Asp Leu Gly Ala Leu Ala Val Arg Tyr Gly Ser Asp 165 170 175 Lys Trp Ala Asp Leu His Trp Tyr Thr Glu His Tyr Glu His His Phe 180 185 190 Ser Arg Phe Gln Asp Ala Pro Val Arg Val Leu Glu Ile Gly Ile Gly 195 200 205 Gly Tyr His Ala Pro Glu Leu Gly Gly Ala Ser Leu Arg Met Trp Gln 210 215 220 Arg Tyr Phe Arg Arg Gly Leu Val Tyr Gly Leu Asp Ile Phe Glu Lys 225 230 235 240 Ala Gly Asn Glu Gly His Arg Val Arg Lys Leu Arg Gly Asp Gln Ser 245 250 255 Asp Ala Glu Phe Leu Glu Asp Met Val Ala Lys Ile Gly Pro Phe Asp 260 265 270 Ile Val Ile Asp Asp Gly Ser His Val Asn Asp His Val Lys Lys Ser 275 280 285 Phe Gln Ser Leu Phe Pro His Val Arg Pro Gly Gly Leu Tyr Val Ile 290 295 300 Glu Asp Leu Gln Thr Ala Tyr Trp Pro Gly Tyr Gly Gly Arg Asp Gly 305 310 315 320 Glu Pro Ala Ala Gln Arg Thr Ser Ile Asp Met Leu Lys Glu Leu Ile 325 330 335 Asp Gly Leu His Tyr Gln Glu Arg Glu Ser Arg Cys Gly Thr Glu Pro 340 345 350 Ser Tyr Thr Glu Arg Asn Val Ala Ala Leu His Phe Tyr His Asn Leu 355 360 365 Val Phe Val Glu Lys Gly Leu Asn Ala Glu Thr Ala Ala Pro Gly Phe 370 375 380 Val Pro Arg Gln Ala Leu Gly Val Glu Gly Gly 385 390 395 11 539 PRT Saccharopolyspora spinosa 11 Met Ile Ser Ala Ala Gly Glu Gln Ser Gly Pro Val Arg Lys Gly Gly 1 5 10 15 Ala Val Pro Glu Phe His Asp Pro Ala Pro Met Asn Arg Arg Thr Pro 20 25 30 Gly Thr Glu Ile Thr Val Glu Pro Asp Asp Pro Arg Tyr Pro Asp Leu 35 40 45 Val Val Gly His Asn Pro Arg Phe Thr Gly Lys Pro Glu Arg Ile His 50 55 60 Ile Ala Ser Ser Ala Glu Asp Val Val His Ala Val Ala Asp Ala Val 65 70 75 80 Arg Thr Gly Arg Arg Val Gly Val Arg Ser Gly Gly His Cys Phe Glu 85 90 95 Asn Leu Val Ala Asp Pro Ala Ile Arg Val Leu Val Asp Leu Ser Glu 100 105 110 Leu Asn Arg Val Tyr Tyr Asp Ser Thr Arg Gly Ala Phe Ala Ile Glu 115 120 125 Ala Gly Ala Ala Leu Gly Gln Val Tyr Arg Thr Leu Phe Lys Asn Trp 130 135 140 Gly Val Thr Ile Pro Thr Gly Ala Cys Pro Gly Val Gly Ala Gly Gly 145 150 155 160 His Ile Leu Gly Gly Gly Tyr Gly Pro Leu Ser Arg Arg Phe Gly Ser 165 170 175 Val Val Asp Tyr Leu Gln Gly Val Glu Val Val Val Val Asp Gln Ala 180 185 190 Gly Glu Val His Ile Val Glu Ala Asp Arg Asn Ser Thr Gly Ala Gly 195 200 205 His Asp Leu Trp Trp Ala His Thr Gly Gly Gly Gly Gly Asn Phe Gly 210 215 220 Ile Val Thr Arg Phe Trp Leu Arg Thr Pro Asp Val Val Ser Thr Asp 225 230 235 240 Ala Ala Glu Leu Leu Pro Arg Pro Pro Ala Thr Val Leu Leu Arg Ser 245 250 255 Phe His Trp Pro Trp His Glu Leu Thr Glu Gln Ser Phe Ala Val Leu 260 265 270 Leu Gln Asn Phe Gly Asn Trp Tyr Glu Gln His Ser Ala Pro Glu Ser 275 280 285 Thr Gln Leu Gly Leu Phe Ser Thr Leu Val Cys Ala His Arg Gln Ala 290 295 300 Gly Tyr Val Thr Leu Asn Val His Leu Asp Gly Thr Asp Pro Asn Ala 305 310 315 320 Glu Arg Thr Leu Ala Glu His Leu Ser Ala Ile Asn Ala Gln Val Gly 325 330 335 Val Thr Pro Ala Glu Gly Leu Arg Glu Thr Leu Pro Trp Leu Arg Ser 340 345 350 Thr Gln Val Ala Gly Ala Ile Ala Glu Gly Gly Glu Pro Gly Met Gln 355 360 365 Arg Thr Lys Val Lys Ala Ala Tyr Leu Arg Thr Gly Leu Ser Glu Ala 370 375 380 Gln Leu Ala Thr Val Tyr Arg Arg Leu Thr Val Tyr Gly Tyr Asp Asn 385 390 395 400 Pro Ala Ala Ala Leu Leu Leu Leu Gly Tyr Gly Gly Met Ala Asn Ala 405 410 415 Val Ala Pro Ser Ala Thr Ala Leu Ala Gln Arg Asp Ser Val Leu Lys 420 425 430 Ala Leu Phe Val Thr Asn Trp Ser Glu Pro Ala Glu Asp Glu Arg His 435 440 445 Leu Thr Trp Ile Arg Gly Phe Tyr Arg Glu Met Tyr Ala Glu Thr Gly 450 455 460 Gly Val Pro Val Pro Gly Thr Arg Val Asp Gly Ser Tyr Ile Asn Tyr 465 470 475 480 Pro Asp Thr Asp Leu Ala Asp Pro Leu Trp Asn Thr Ser Gly Val Ala 485 490 495 Trp His Asp Leu Tyr Tyr Lys Asp Asn Tyr Pro Arg Leu Gln Arg Ala 500 505 510 Lys Ala Arg Trp Asp Pro Gln Asn Ile Phe Gln His Gly Leu Ser Ile 515 520 525 Lys Pro Pro Ala Arg Leu Ser Pro Gly Gln Pro 530 535 12 397 PRT Saccharopolyspora spinosa 12 Met Ser Thr Thr His Glu Ile Glu Thr Val Glu Arg Ile Ile Leu Ala 1 5 10 15 Ala Gly Ser Ser Ala Ala Ser Leu Ala Asp Leu Thr Thr Glu Leu Gly 20 25 30 Leu Ala Arg Ile Ala Pro Val Leu Ile Asp Glu Ile Leu Phe Arg Ala 35 40 45 Glu Pro Ala Pro Asp Ile Glu Arg Thr Glu Val Ala Val Gln Ile Thr 50 55 60 His Arg Gly Glu Thr Val Asp Phe Val Leu Thr Leu Gln Ser Gly Glu 65 70 75 80 Leu Ile Lys Ala Glu Gln Arg Pro Val Gly Asp Val Pro Leu Arg Ile 85 90 95 Gly Tyr Glu Leu Thr Asp Leu Ile Ala Glu Leu Phe Gly Pro Gly Ala 100 105 110 Pro Arg Ala Val Gly Ala Arg Ser Thr Asn Phe Leu Arg Thr Thr Thr 115 120 125 Ser Gly Ser Ile Pro Gly Pro Ser Glu Leu Ser Asp Gly Phe Gln Ala 130 135 140 Ile Ser Ala Val Val Ala Gly Cys Gly His Arg Arg Pro Asp Leu Asn 145 150 155 160 Leu Leu Ala Ser His Tyr Arg Thr Asp Lys Trp Gly Gly Leu His Trp 165 170 175 Phe Thr Pro Leu Tyr Glu Arg His Leu Gly Glu Phe Arg Asp Arg Pro 180 185 190 Val Arg Ile Leu Glu Ile Gly Val Gly Gly Tyr Asn Phe Asp Gly Gly 195 200 205 Gly Gly Glu Ser Leu Lys Met Trp Lys Arg Tyr Phe His Arg Gly Leu 210 215 220 Val Phe Gly Met Asp Val Phe Asp Lys Ser Phe Leu Asp Gln Gln Arg 225 230 235 240 Leu Cys Thr Val Arg Ala Asp Gln Ser Lys Pro Glu Glu Leu Ala Ala 245 250 255 Val Asp Asp Lys Tyr Gly Pro Phe Asp Ile Ile Ile Asp Asp Gly Ser 260 265 270 His Ile Asn Gly His Val Arg Thr Ser Leu Glu Thr Leu Phe Pro Arg 275 280 285 Leu Arg Ser Gly Gly Val Tyr Val Ile Glu Asp Leu Trp Thr Thr Tyr 290 295 300 Ala Pro Gly Phe Gly Gly Gln Ala Gln Cys Pro Ala Ala Pro Gly Thr 305 310 315 320 Thr Val Ser Leu Leu Lys Asn Leu Leu Glu Gly Val Gln His Glu Glu 325 330 335 Gln Pro His Ala Gly Ser Tyr Glu Pro Ser Tyr Leu Glu Arg Asn Leu 340 345 350 Val Gly Leu His Thr Tyr His Asn Ile Ala Phe Leu Glu Lys Gly Val 355 360 365 Asn Ala Glu Gly Gly Val Pro Ala Trp Val Pro Arg Ser Leu Asp Asp 370 375 380 Ile Leu His Leu Ala Asp Val Asn Ser Ala Glu Asp Glu 385 390 395 13 283 PRT Saccharopolyspora spinosa 13 Val Glu Ser Ile Phe Asp Ala Leu Ala His Gly Arg Pro Leu His His 1 5 10 15 Gly Tyr Trp Ala Gly Gly Tyr Arg Glu Asp Ala Gly Ala Thr Pro Trp 20 25 30 Ser Asp Ala Ala Asp Gln Leu Thr Asp Leu Phe Ile Asp Lys Ala Ala 35 40 45 Leu Arg Pro Gly Ala His Leu Phe Asp Leu Gly Cys Gly Asn Gly Gln 50 55 60 Pro Val Val Arg Ala Ala Cys Ala Ser Gly Val Arg Val Thr Gly Ile 65 70 75 80 Thr Val Asn Ala Gln His Leu Ala Ala Ala Thr Arg Leu Ala Asn Glu 85 90 95 Thr Gly Leu Ala Gly Ser Leu Glu Phe Asp Leu Val Asp Gly Ala Gln 100 105 110 Leu Pro Tyr Pro Asp Gly Phe Phe Gln Ala Ala Trp Ala Met Gln Ser 115 120 125 Val Val Gln Ile Val Asp Gln Ala Ala Ala Ile Arg Glu Val His Arg 130 135 140 Ile Leu Glu Pro Gly Gly Arg Phe Val Leu Gly Asp Ile Ile Thr Arg 145 150 155 160 Val Arg Leu Pro Glu Glu Tyr Ala Ala Val Trp Thr Gly Thr Thr Ala 165 170 175 His Thr Leu Asn Ser Phe Thr Ala Leu Val Ser Glu Ala Gly Phe Glu 180 185 190 Ile Leu Glu Val Thr Asp Leu Thr Ala Gln Thr Arg Cys Met Val Ser 195 200 205 Trp Tyr Val Asp Glu Leu Leu Arg Lys Leu Asp Glu Leu Ala Gly Val 210 215 220 Glu Pro Ala Ala Val Gly Thr Tyr Gln Gln Arg Tyr Leu Gly Asp Ile 225 230 235 240 Ala Ala Lys His Gly Pro Gly Pro Ala Gln Leu Ile Ala Ala Val Ala 245 250 255 Glu Tyr Arg Lys His Pro Asp Tyr Ala Arg Asn Glu Glu Ser Met Gly 260 265 270 Phe Met Leu Leu Gln Ala Arg Lys Lys Gln Ser 275 280 14 320 PRT Saccharopolyspora spinosa 14 Met Pro Asn Ala Val Ser Gly Thr Val Leu Val Pro Asn Ile Pro Trp 1 5 10 15 Pro Arg Glu Asp Arg Pro Ile Ile Thr Phe Ala Val Gly Thr His Gly 20 25 30 Leu Gly Ser Gln Val Ala Pro Ser Tyr Leu Leu Arg Thr Gly Thr Glu 35 40 45 Pro Glu Thr Glu Leu Ile Ala Val Ala Leu Asp Arg Gly Trp Ala Val 50 55 60 Val Ile Thr Asp Tyr Glu Gly Leu Gly Thr Pro Gly Thr His Thr Tyr 65 70 75 80 Thr Val Gly Arg Ala Gln Gly His Ala Met Leu Asp Ala Ala Arg Ala 85 90 95 Ala Gln Arg Leu Pro Gly Ser Gly Leu Thr Thr Asp Cys Pro Val Gly 100 105 110 Ile Trp Gly Tyr Ala Gln Gly Gly Gln Ala Ser Ala Phe Ala Gly Glu 115 120 125 Leu His Pro Thr Tyr Ala Pro Glu Leu Arg Ile Arg Ala Ala Ala Ala 130 135 140 Gly Ala Val Pro Ile Asp Leu Leu Asp Ile Ile His Arg Asn Asp Gly 145 150 155 160 Val Phe Thr Gly Pro Val Leu Ala Gly Leu Val Gly His Ala Ala Ala 165 170 175 Tyr Pro Asp Leu Pro Phe Asp Glu Leu Leu Thr Glu Ala Gly Arg Thr 180 185 190 Ala Val Asp Gln Val Arg Glu Leu Gly Ala Pro Glu Leu Val Thr Arg 195 200 205 Phe Leu Gly Arg Glu Leu Ser Asp Phe Leu Asp Thr Ser Gly Leu Phe 210 215 220 Glu Gln Pro Arg Trp Arg Ala Arg Leu Ala Glu Ser Val Ala Gly Arg 225 230 235 240 Asn Gly Gly Pro Val Val Pro Thr Leu Val Tyr His Ser Thr Asp Asp 245 250 255 Glu Ile Val Pro Phe Ala Phe Gly Glu Arg Leu Arg Asp Ser Tyr Arg 260 265 270 Ala Ala Gly Thr Pro Val Arg Trp His Pro Leu Ser Gly Leu Ala His 275 280 285 Phe Pro Ala Ala Leu Ala Ser Ser Arg Val Val Val Ser Trp Phe Asp 290 295 300 Glu His Phe Ser Glu Pro Ser Ala Ile Ser Gly Pro Arg Asp Ala Arg 305 310 315 320 15 332 PRT Saccharopolyspora spinosa 15 Met Arg Lys Pro Val Arg Ile Gly Val Leu Gly Cys Ala Ser Phe Ala 1 5 10 15 Trp Arg Arg Met Leu Pro Ala Met Cys Asp Val Ala Glu Thr Glu Val 20 25 30 Val Ala Val Ala Ser Arg Asp Pro Ala Lys Ala Glu Arg Phe Ala Ala 35 40 45 Arg Phe Glu Cys Glu Ala Val Leu Gly Tyr Gln Arg Leu Leu Glu Arg 50 55 60 Pro Asp Ile Asp Ala Val Tyr Val Pro Leu Pro Pro Gly Met His Ala 65 70 75 80 Glu Trp Ile Gly Lys Ala Leu Glu Ala Asp Lys His Val Leu Ala Glu 85 90 95 Lys Pro Leu Thr Thr Thr Ala Ser Asp Thr Ala Arg Leu Val Gly Leu 100 105 110 Ala Arg Arg Lys Asn Leu Leu Leu Arg Glu Asn Tyr Leu Phe Leu His 115 120 125 His Gly Arg His Asp Val Val Arg Asp Leu Leu Gln Ser Gly Glu Ile 130 135 140 Gly Glu Leu Arg Glu Phe Thr Ala Val Phe Gly Ile Pro Pro Leu Pro 145 150 155 160 Asp Thr Asp Ile Arg Tyr Arg Thr Glu Leu Gly Gly Gly Ala Leu Leu 165 170 175 Asp Ile Gly Val Tyr Pro Ala Arg Ala Ala Arg His Phe Leu Leu Gly 180 185 190 Pro Leu Thr Val Leu Gly Ala Ser Ser His Glu Ala Gln Glu Ser Gly 195 200 205 Val Asp Leu Ser Gly Ser Val Leu Leu Gln Ser Glu Gly Gly Thr Val 210 215 220 Ala His Leu Gly Tyr Gly Phe Val His His Tyr Arg Ser Ala Tyr Glu 225 230 235 240 Leu Trp Gly Ser Arg Gly Arg Ile Val Val Asp Arg Ala Phe Thr Pro 245 250 255 Pro Ala Glu Trp Gln Ala Val Ile Arg Ile Glu Arg Lys Gly Val Val 260 265 270 Asp Glu Leu Ser Leu Pro Ala Glu Asp Gln Val Arg Lys Ala Val Thr 275 280 285 Ala Phe Ala Arg Asp Ile Arg Ala Gly Thr Gly Val Asp Asp Pro Ala 290 295 300 Val Ala Gly Asp Ser Gly Glu Ser Met Ile Gln Gln Ala Ala Leu Val 305 310 315 320 Glu Ala Ile Gly Gln Ala Arg Arg Cys Gly Ser Thr 325 330 16 486 PRT Saccharopolyspora spinosa 16 Met Ser Ser Ser Val Glu Ala Glu Ala Ser Ala Ala Ala Pro Leu Gly 1 5 10 15 Ser Asn Asn Thr Arg Arg Phe Val Asp Ser Ala Leu Ser Ala Cys Asn 20 25 30 Gly Met Ile Pro Thr Thr Glu Phe His Cys Trp Leu Ala Asp Arg Leu 35 40 45 Gly Glu Asn Ser Phe Glu Thr Asn Arg Ile Pro Phe Asp Arg Leu Ser 50 55 60 Lys Trp Lys Phe Asp Ala Ser Thr Glu Asn Leu Val His Ala Asp Gly 65 70 75 80 Arg Phe Phe Thr Val Glu Gly Leu Gln Val Glu Thr Asn Tyr Gly Ala 85 90 95 Ala Pro Ser Trp His Gln Pro Ile Ile Asn Gln Ala Glu Val Gly Ile 100 105 110 Leu Gly Ile Leu Val Lys Glu Ile Asp Gly Val Leu His Cys Leu Met 115 120 125 Ser Ala Lys Met Glu Pro Gly Asn Val Asn Val Leu Gln Leu Ser Pro 130 135 140 Thr Val Gln Ala Thr Arg Ser Asn Tyr Thr Gln Ala His Arg Gly Ser 145 150 155 160 Val Pro Pro Tyr Val Asp Tyr Phe Leu Gly Arg Gly Arg Gly Arg Val 165 170 175 Leu Val Asp Val Leu Gln Ser Glu Gln Gly Ser Trp Phe Tyr Arg Lys 180 185 190 Arg Asn Arg Asn Met Val Val Glu Val Gln Glu Glu Val Pro Val Leu 195 200 205 Pro Asp Phe Cys Trp Leu Thr Leu Gly Gln Val Leu Ala Leu Leu Arg 210 215 220 Gln Asp Asn Ile Val Asn Met Asp Thr Arg Thr Val Leu Ser Cys Ile 225 230 235 240 Pro Phe His Asp Ser Ala Thr Gly Pro Glu Leu Ala Ala Ser Glu Glu 245 250 255 Pro Phe Arg Gln Ala Val Ala Arg Ser Leu Ser His Gly Ile Asp Ser 260 265 270 Ser Ser Ile Ser Glu Ala Val Gly Trp Phe Glu Glu Ala Lys Ala Arg 275 280 285 Tyr Arg Leu Arg Ala Thr Arg Val Pro Leu Ser Arg Val Asp Lys Trp 290 295 300 Tyr Arg Thr Asp Thr Glu Ile Ala His Gln Asp Gly Lys Tyr Phe Ala 305 310 315 320 Val Ile Ala Val Ser Val Ser Ala Thr Asn Arg Glu Val Ala Ser Trp 325 330 335 Thr Gln Pro Met Ile Glu Pro Arg Glu Gln Gly Glu Ile Ala Leu Leu 340 345 350 Val Lys Arg Ile Gly Gly Val Leu His Gly Leu Val His Ala Arg Val 355 360 365 Glu Ala Gly Tyr Lys Trp Thr Ala Glu Ile Ala Pro Thr Val Gln Cys 370 375 380 Ser Val Ala Asn Tyr Gln Ser Thr Pro Ser Asn Asp Trp Pro Pro Phe 385 390 395 400 Leu Asp Asp Val Leu Thr Ala Asp Pro Glu Thr Val Arg Tyr Glu Ser 405 410 415 Ile Leu Ser Glu Glu Gly Gly Arg Phe Tyr Gln Ala Gln Asn Arg Tyr 420 425 430 Arg Ile Ile Glu Val His Glu Asp Phe Ala Ala Arg Pro Pro Ser Asp 435 440 445 Phe Arg Trp Met Thr Leu Gly Gln Leu Gly Glu Leu Leu Arg Ser Thr 450 455 460 His Phe Leu Asn Ile Gln Ala Arg Ser Leu Val Ala Ser Leu His Ser 465 470 475 480 Leu Trp Ala Leu Gly Arg 485 17 455 PRT Saccharopolyspora spinosa 17 Val Ile Leu Gly Met Leu Pro Gly Cys Ser Ile Ala Ile Gly Glu Phe 1 5 10 15 Met Arg Val Leu Phe Thr Pro Leu Pro Ala Ser Ser His Phe Phe Asn 20 25 30 Leu Val Pro Leu Ala Trp Ala Leu Arg Ala Ala Gly His Glu Val Arg 35 40 45 Val Ala Ile Cys Pro Asn Met Val Ser Met Val Thr Gly Ala Gly Leu 50 55 60 Thr Ala Val Pro Val Gly Asp Glu Leu Asp Leu Ile Ser Leu Ala Ala 65 70 75 80 Lys Asn Glu Leu Val Leu Gly Ser Gly Val Ser Phe Asp Glu Lys Gly 85 90 95 Arg His Pro Glu Leu Phe Asp Glu Leu Leu Ser Ile Asn Ser Gly Arg 100 105 110 Asp Thr Asp Ala Val Glu Gln Leu His Leu Val Asp Asp Arg Ser Leu 115 120 125 Asp Asp Leu Met Gly Phe Ala Glu Lys Trp Gln Pro Asp Leu Val Val 130 135 140 Trp Asp Ala Met Val Cys Ser Gly Pro Val Val Ala Arg Ala Leu Gly 145 150 155 160 Ala Arg His Val Arg Met Leu Val Ala Leu Asp Val Ser Gly Trp Leu 165 170 175 Arg Ser Gly Phe Leu Glu Tyr Gln Glu Ser Lys Pro Pro Glu Gln Arg 180 185 190 Val Asp Pro Leu Gly Thr Trp Leu Gly Ala Lys Leu Ala Lys Phe Gly 195 200 205 Ala Thr Phe Asp Glu Glu Ile Val Thr Gly Gln Ala Thr Ile Asp Pro 210 215 220 Ile Pro Ser Trp Met Arg Leu Pro Val Asp Leu Asp Tyr Ile Ser Met 225 230 235 240 Arg Phe Val Pro Tyr Asn Gly Pro Ala Val Leu Pro Glu Trp Leu Arg 245 250 255 Glu Arg Pro Thr Lys Pro Arg Val Cys Ile Thr Arg Gly Leu Thr Lys 260 265 270 Arg Arg Leu Ser Arg Val Thr Glu Gln Tyr Gly Glu Gln Ser Asp Gln 275 280 285 Glu Gln Ala Met Val Glu Arg Leu Leu Arg Gly Ala Ala Arg Leu Asp 290 295 300 Val Glu Val Ile Ala Thr Leu Ser Asp Asp Glu Val Arg Glu Met Gly 305 310 315 320 Glu Leu Pro Ser Asn Val Arg Val His Glu Tyr Val Pro Leu Asn Glu 325 330 335 Leu Leu Glu Ser Cys Ser Val Ile Ile His His Gly Ser Thr Thr Thr 340 345 350 Gln Glu Thr Ala Thr Val Asn Gly Val Pro Gln Leu Ile Leu Pro Gly 355 360 365 Thr Phe Trp Asp Glu Ser Arg Arg Ala Glu Leu Leu Ala Asp Arg Gly 370 375 380 Ala Gly Leu Val Leu Asp Pro Ala Thr Phe Thr Glu Asp Asp Val Arg 385 390 395 400 Gly Gln Leu Ala Arg Leu Leu Asp Glu Pro Ser Phe Ala Ala Asn Ala 405 410 415 Ala Leu Ile Arg Arg Glu Ile Glu Glu Ser Pro Ser Pro His Asp Ile 420 425 430 Val Pro Arg Leu Glu Lys Leu Val Ala Glu Arg Glu Asn Arg Arg Thr 435 440 445 Gly Gln Ser Asp Gly His Pro 450 455 18 462 PRT Saccharopolyspora spinosa 18 Met Gln Ser Arg Lys Thr Arg Ala Leu Gly Lys Gly Arg Ala Arg Val 1 5 10 15 Thr Ser Cys Asp Asp Thr Cys Ala Thr Ala Thr Glu Met Val Pro Asp 20 25 30 Ala Lys Asp Arg Ile Leu Ala Ser Val Arg Asp Tyr His Arg Glu Gln 35 40 45 Glu Ser Pro Thr Phe Val Ala Gly Ser Thr Pro Ile Arg Pro Ser Gly 50 55 60 Ala Val Leu Asp Glu Asp Asp Arg Val Ala Leu Val Glu Ala Ala Leu 65 70 75 80 Glu Leu Arg Ile Ala Ala Gly Gly Asn Ala Arg Arg Phe Glu Ser Glu 85 90 95 Phe Ala Arg Phe Phe Gly Leu Arg Lys Ala His Leu Val Asn Ser Gly 100 105 110 Ser Ser Ala Asn Leu Leu Ala Leu Ser Ser Leu Thr Ser Pro Lys Leu 115 120 125 Gly Glu Ala Arg Leu Arg Pro Gly Asp Glu Val Ile Thr Ala Ala Val 130 135 140 Gly Phe Pro Thr Thr Ile Asn Pro Ala Val Gln Asn Gly Leu Val Pro 145 150 155 160 Val Phe Val Asp Val Glu Leu Gly Thr Tyr Asn Ala Thr Pro Asp Arg 165 170 175 Ile Lys Ala Ala Val Thr Glu Arg Thr Arg Ala Ile Met Leu Ala His 180 185 190 Thr Leu Gly Asn Pro Phe Ala Ala Asp Glu Ile Ala Glu Ile Ala Lys 195 200 205 Glu His Glu Leu Phe Leu Val Glu Asp Asn Cys Asp Ala Val Gly Ser 210 215 220 Thr Tyr Arg Gly Arg Leu Thr Gly Thr Phe Gly Asp Leu Thr Thr Val 225 230 235 240 Ser Phe Tyr Pro Ala His His Ile Thr Ser Gly Glu Gly Gly Cys Val 245 250 255 Leu Thr Gly Ser Leu Glu Leu Ala Arg Ile Ile Glu Ser Leu Arg Asp 260 265 270 Trp Gly Arg Asp Cys Trp Cys Glu Pro Gly Val Asp Asn Thr Cys Arg 275 280 285 Lys Arg Phe Asp Tyr His Leu Gly Thr Leu Pro Pro Gly Tyr Asp His 290 295 300 Lys Tyr Thr Phe Ser His Val Gly Tyr Asn Leu Lys Thr Thr Asp Leu 305 310 315 320 Gln Ala Ala Leu Ala Leu Ser Gln Leu Ser Lys Ile Ser Ala Phe Gly 325 330 335 Ser Ala Arg Arg Arg Asn Trp Arg Arg Leu Arg Glu Gly Leu Ser Gly 340 345 350 Leu Pro Gly Leu Leu Leu Pro Val Ala Thr Pro His Ser Asp Pro Ser 355 360 365 Trp Phe Gly Phe Ala Ile Thr Ile Ser Ala Asp Ala Gly Phe Thr Arg 370 375 380 Ala Ala Leu Val Asn Phe Leu Glu Ser Arg Asn Ile Gly Thr Arg Leu 385 390 395 400 Leu Phe Gly Gly Asn Ile Thr Arg His Pro Ala Phe Glu Gln Val Arg 405 410 415 Tyr Arg Ile Ala Asp Ala Leu Thr Asn Ser Asp Ile Val Thr Asp Arg 420 425 430 Thr Phe Trp Val Gly Val Tyr Pro Gly Ile Thr Asp Gln Met Ile Asp 435 440 445 Tyr Val Val Glu Ser Ile Ala Glu Phe Val Ala Lys Ser Ser 450 455 460 19 385 PRT Saccharopolyspora spinosa 19 Val Ile Asn Leu His Gln Pro Ile Leu Gly Thr Glu Glu Leu Asp Ala 1 5 10 15 Ile Ala Glu Val Phe Ala Ser Asn Trp Ile Gly Leu Gly Pro Arg Thr 20 25 30 Arg Thr Phe Glu Ala Glu Phe Ala His His Leu Gly Val Asp Pro Glu 35 40 45 Gln Val Val Phe Leu Asn Ser Gly Thr Ala Ala Leu Phe Leu Thr Val 50 55 60 Gln Val Leu Asp Leu Gly Pro Gly Asp Asp Val Val Leu Pro Ser Ile 65 70 75 80 Ser Phe Val Ala Ala Ala Asn Ala Ile Ala Ser Ser Gly Ala Arg Pro 85 90 95 Val Phe Cys Asp Val Asp Pro Arg Thr Leu Asn Pro Thr Leu Asp Asp 100 105 110 Val Ala Arg Ala Ile Thr Pro Ala Thr Lys Ala Val Leu Leu Leu His 115 120 125 Tyr Gly Gly Ser Pro Gly Glu Val Thr Ala Ile Ala Asp Phe Cys Arg 130 135 140 Glu Lys Gly Leu Met Leu Ile Glu Asp Ser Ala Cys Ala Val Ala Ser 145 150 155 160 Ser Val His Gly Thr Ala Cys Gly Thr Phe Gly Asp Leu Ala Thr Trp 165 170 175 Ser Phe Asp Ala Met Lys Ile Leu Val Thr Gly Asp Gly Gly Met Phe 180 185 190 Tyr Ala Ala Asp Pro Glu Leu Ala His Arg Ala Arg Arg Leu Ala Tyr 195 200 205 His Gly Leu Glu Gln Met Ser Gly Phe Asp Ser Ala Lys Ser Ser Asn 210 215 220 Arg Trp Trp Asp Ile Arg Val Glu Asp Ile Gly Gln Arg Leu Ile Gly 225 230 235 240 Asn Asp Met Thr Ala Ala Leu Gly Ser Val Gln Leu Arg Lys Leu Pro 245 250 255 Glu Phe Ile Asn Arg Arg Arg Glu Ile Ala Thr Gln Tyr Asp Arg Leu 260 265 270 Leu Ser Asp Val Pro Gly Val Leu Leu Pro Pro Thr Leu Pro Asp Gly 275 280 285 His Val Ser Ser His Tyr Phe Tyr Trp Val Gln Leu Ala Pro Glu Ile 290 295 300 Arg Asp Gln Val Ala Gln Gln Met Leu Glu Arg Gly Ile Tyr Thr Ser 305 310 315 320 Tyr Arg Tyr Pro Pro Leu His Lys Val Pro Ile Tyr Arg Ala Asp Cys 325 330 335 Lys Leu Pro Ser Ala Glu Asp Ala Cys Arg Arg Thr Leu Leu Leu Pro 340 345 350 Leu His Pro Ser Leu Asp Asp Ala Glu Val Arg Thr Val Ala Asp Glu 355 360 365 Phe Gln Lys Ala Val Glu His His Ile Ser Gln Arg Ser Pro Leu Arg 370 375 380 Lys 385 20 249 PRT Saccharopolyspora spinosa 20 Met Ser Arg Val Ser Asp Thr Phe Ala Glu Thr Ser Ser Val Tyr Ser 1 5 10 15 Pro Asp His Ala Asp Ile Tyr Asp Ala Ile His Ser Ala Arg Gly Arg 20 25 30 Asp Trp Ala Ala Glu Ala Gly Glu Val Val Gln Leu Val Arg Thr Arg 35 40 45 Leu Pro Glu Ala Gln Ser Leu Leu Asp Val Ala Cys Gly Thr Gly Ala 50 55 60 His Leu Glu Arg Phe Arg Ala Glu Tyr Ala Lys Val Ala Gly Leu Glu 65 70 75 80 Leu Ser Asp Ala Met Arg Glu Ile Ala Ile Arg Arg Val Pro Glu Val 85 90 95 Pro Ile His Ile Gly Asp Ile Arg Asp Phe Asp Leu Gly Glu Pro Phe 100 105 110 Asp Val Ile Thr Cys Leu Cys Phe Thr Ala Ala Tyr Met Arg Thr Val 115 120 125 Asp Asp Leu Arg Arg Val Thr Arg Asn Met Ala Arg His Leu Ala Pro 130 135 140 Gly Gly Val Ala Val Ile Glu Pro Trp Trp Phe Pro Asp Lys Phe Ile 145 150 155 160 Asp Gly Phe Val Thr Gly Ala Val Ala His His Gly Glu Arg Val Ile 165 170 175 Ser Arg Leu Ser His Ser Val Leu Glu Gly Arg Thr Ser Arg Met Thr 180 185 190 Val Arg Tyr Thr Val Ala Glu Pro Thr Gly Ile Arg Asp Phe Thr Glu 195 200 205 Phe Glu Ile Leu Ser Leu Phe Thr Glu Asp Glu Tyr Thr Ala Ala Leu 210 215 220 Glu Asp Ala Gly Ile Arg Ala Glu Tyr Leu Pro Gly Ala Pro Asn Gly 225 230 235 240 Arg Gly Leu Phe Val Gly Ile Arg Asn 245 21 255 PRT Saccharopolyspora spinosa 21 Met Val Leu Val Pro Arg Arg Phe Arg Ala Thr Leu Glu Ser Met Ser 1 5 10 15 Glu Gln Thr Ile Ala Leu Val Thr Gly Ala Asn Lys Gly Ile Gly Tyr 20 25 30 Glu Ile Ala Ala Gly Leu Gly Ala Leu Gly Trp Ser Val Gly Ile Gly 35 40 45 Ala Arg Asp His Gln Arg Gly Glu Asp Ala Val Ala Lys Leu Arg Ala 50 55 60 Asp Gly Val Asp Ala Phe Ala Val Ser Leu Asp Val Thr Asp Asp Ala 65 70 75 80 Ser Val Ala Ala Ala Ala Ala Leu Leu Glu Glu Arg Ala Gly Arg Leu 85 90 95 Asp Val Leu Val Asn Asn Ala Gly Ile Ala Gly Ala Trp Pro Glu Glu 100 105 110 Pro Ser Thr Val Thr Pro Ala Ser Leu Arg Ala Val Val Glu Thr Asn 115 120 125 Val Ile Gly Val Val Arg Val Thr Asn Ala Met Leu Pro Leu Leu Arg 130 135 140 Arg Ser Glu Arg Pro Arg Ile Val Asn Gln Ser Ser His Val Ala Ser 145 150 155 160 Leu Thr Leu Gln Thr Thr Pro Gly Val Asp Leu Gly Gly Ile Ser Gly 165 170 175 Ala Tyr Ser Pro Ser Lys Thr Phe Leu Asn Ala Ile Thr Ile Gln Tyr 180 185 190 Ala Lys Glu Leu Ser Asp Thr Asn Ile Lys Ile Asn Asn Ala Cys Pro 195 200 205 Gly Tyr Val Ala Thr Asp Leu Asn Gly Phe His Gly Thr Ser Thr Pro 210 215 220 Ala Asp Gly Ala Arg Ile Ala Ile Arg Leu Ala Thr Leu Pro Asp Asp 225 230 235 240 Gly Pro Thr Gly Gly Met Phe Asp Asp Ala Gly Asn Val Pro Trp 245 250 255 22 278 PRT Saccharopolyspora spinosa 22 Met Glu Thr Arg Glu Leu Arg Tyr Phe Val Ala Val Ala Glu Glu Leu 1 5 10 15 His Phe Gly Arg Ala Ala Gln Arg Leu Gly Ile Ala Gln Pro Pro Leu 20 25 30 Ser Arg Thr Ile Ala Gln Leu Glu Gln Arg Leu Gly Val Val Leu Leu 35 40 45 Gln Arg Thr Ser Arg Lys Val Ser Leu Thr Glu Ala Gly Ala Met Leu 50 55 60 Leu Thr Glu Gly Arg Ala Ile Leu Gly Ala Leu Ala Ala Ala Glu Arg 65 70 75 80 Arg Thr Gln Arg Ala Ala Thr Ser Gln Pro Ser Leu Val Leu Ala Ala 85 90 95 Lys Ala Gly Ala Ser Gly Glu Leu Leu Ala Lys Leu Leu Asp Ala Tyr 100 105 110 Ala Ala Glu Pro Gly Ala Val Ala Val Asp Leu Leu Leu Cys Glu Ser 115 120 125 Gln Pro Gln Lys Thr Leu His Asp Gly Arg Ala Asp Val Ala Leu Leu 130 135 140 His Gln Pro Phe Asp Pro Thr Ala Glu Leu Asp Ile Glu Ile Leu Asn 145 150 155 160 Thr Glu Gln Gln Val Ala Ile Leu Pro Thr Ser His Pro Leu Ala Ser 165 170 175 Glu Pro His Val Arg Met Ala Asp Val Ser Ser Leu Pro Asp Leu Pro 180 185 190 Leu Ala Arg Trp Pro Gly Pro Asp Gly Val Tyr Pro Asp Gly Pro Gly 195 200 205 Val Glu Val Arg Asn Gln Thr Gln Leu Phe Gln Met Ile Ala Leu Gly 210 215 220 Arg Thr Thr Val Val Met Pro Glu Ser Ser Arg Val Asn Leu Leu Glu 225 230 235 240 Gly Leu Ala Ala Val Pro Val Leu Asp Ala Pro Asp Val Thr Thr Val 245 250 255 Ile Ala Trp Pro Pro His Ser Arg Ser Arg Ala Leu Ala Gly Leu Val 260 265 270 Arg Val Ala Thr Leu Leu 275 23 198 PRT Saccharopolyspora spinosa 23 Met Met Leu Lys Arg His Arg Leu Thr Thr Ala Ile Thr Gly Leu Leu 1 5 10 15 Gly Gly Val Leu Leu Val Ser Gly Cys Gly Thr Ala Ala Ala Leu Gln 20 25 30 Ser Ser Pro Ala Pro Gly His Asp Ala Arg Asn Val Gly Met Ala Ser 35 40 45 Gly Gly Gly Gly Gly Asp Ile Gly Thr Ser Asn Cys Ser Glu Ala Asp 50 55 60 Phe Leu Ala Thr Ala Thr Pro Val Lys Gly Asp Pro Gly Ser Phe Ile 65 70 75 80 Val Ala Tyr Gly Asn Arg Ser Asp Lys Thr Cys Thr Ile Asn Gly Gly 85 90 95 Val Pro Asn Leu Lys Gly Val Asp Met Ser Asn Ser Pro Ile Glu Asp 100 105 110 Leu Pro Val Glu Asp Val Arg Leu Pro Asp Ala Pro Lys Glu Phe Thr 115 120 125 Leu Gln Pro Gly Gln Ser Ala Tyr Ala Gly Ile Gly Met Val Leu Ala 130 135 140 Asp Ser Gly Asp Pro Asn Ala His Val Leu Thr Gly Phe Gln Ser Ser 145 150 155 160 Leu Pro Asp Met Ser Glu Ala Gln Pro Val Asn Val Leu Gly Asp Gly 165 170 175 Asn Val Lys Phe Ala Ala Lys Tyr Leu Arg Val Ser Ser Leu Val Ser 180 185 190 Thr Ala Asp Glu Leu Arg 195 24 751 PRT Saccharopolyspora spinosa 24 Val Leu Ser Val Glu Lys Gly Arg Glu Ser Ala Thr Trp Thr Ala Val 1 5 10 15 Leu Glu Gly Thr Leu Glu Arg Ile Thr Phe Ala Asn Glu Glu Ser Gly 20 25 30 Tyr Thr Val Ala Arg Ile Asp Thr Gly Arg Gly Gly Asp Leu Val Thr 35 40 45 Val Val Gly Ala Leu Leu Gly Ala Gln Pro Gly Glu Ala Leu Arg Met 50 55 60 Arg Gly Arg Trp Gly Ser His Pro Gln Tyr Gly Arg Gln Phe His Val 65 70 75 80 Asp Asp Tyr Thr Thr Val Leu Pro Ala Thr Val Gln Gly Ile Arg Arg 85 90 95 Tyr Leu Gly Ser Gly Leu Ile Lys Gly Ile Gly Pro Lys Leu Ala Glu 100 105 110 Lys Ile Val Asp His Phe Gly Val Ala Ala Leu Asp Val Ile Glu Gln 115 120 125 Glu Pro Ala Arg Leu Ile Glu Val Pro Lys Leu Gly Pro Lys Arg Thr 130 135 140 Lys Leu Ile Ala Asp Ala Trp Glu Glu Gln Lys Ala Ile Lys Glu Val 145 150 155 160 Met Ile Phe Leu Gln Gly Val Gly Val Ser Thr Ser Leu Ala Val Lys 165 170 175 Ile Tyr Lys Gln Tyr His Asp Asp Ala Ile Arg Thr Val Lys Glu Glu 180 185 190 Pro Tyr Arg Leu Ala Gly Asp Val Trp Gly Ile Gly Phe Lys Thr Ala 195 200 205 Asp Thr Ile Ala Lys Ala Val Gly Ile Pro His Asp Ser Pro Gln Arg 210 215 220 Val Lys Ala Gly Leu Gln Phe Thr Leu Ser Glu Ser Thr Gly Asp Gly 225 230 235 240 Asn Cys Tyr Leu Pro Glu Asn Glu Leu Ile Ala Glu Ala Val Lys Ile 245 250 255 Leu Ala Val Asp Thr Gly Leu Val Ile Glu Cys Leu Ala Glu Leu Val 260 265 270 Thr Glu Glu Gly Val Val Arg Glu Glu Ile Pro Thr Asp Asp Asp Glu 275 280 285 Val Pro Thr Val Ala Ile Tyr Leu Val Pro Phe His Arg Ala Glu Val 290 295 300 Ala Leu Ala Asn Gln Leu Ser Arg Leu Leu Asn Thr Ser Ala Asp Arg 305 310 315 320 Met Pro Val Phe Ala Asp Val Asp Trp His Lys Ala Leu Asp Trp Leu 325 330 335 Arg Arg Ala Thr Gly Ala Glu Leu Ala Glu Ala Gln Glu Arg Ala Val 340 345 350 Lys Leu Ala Leu Thr Glu Lys Val Ala Val Leu Thr Gly Gly Pro Gly 355 360 365 Cys Gly Lys Ser Phe Thr Val Arg Ser Ile Ile Ala Leu Ala Gln Ala 370 375 380 Lys Lys Ala Lys Val Ile Leu Ala Ala Pro Thr Gly Arg Ala Ala Lys 385 390 395 400 Arg Leu Thr Glu Leu Thr Gly His Asp Ala Ala Thr Val His Arg Leu 405 410 415 Leu Gln Leu Gln Pro Gly Gly Asp Ala Ala Tyr Asp Arg Asp Asn Pro 420 425 430 Leu Asp Ala Asp Leu Val Val Val Asp Glu Ala Ser Met Leu Asp Leu 435 440 445 Leu Leu Ala Asn Lys Leu Ala Lys Ala Ile Ala Pro Gly Ala His Leu 450 455 460 Leu Leu Val Gly Asp Val Asp Gln Leu Pro Ser Val Gly Ala Gly Glu 465 470 475 480 Val Leu Arg Asp Leu Leu Ala Pro Gly Thr Pro Ile Pro His Val Arg 485 490 495 Leu Asn Glu Val Phe Arg Gln Ala Ala Glu Ser Gly Val Val Thr Asn 500 505 510 Ala His Arg Ile Asn Ala Gly Asp Tyr Pro Leu Thr His Gly Leu Thr 515 520 525 Asp Phe Phe Leu Phe His Val Glu Glu Ser Glu Pro Thr Ala Glu Leu 530 535 540 Thr Val Asp Val Val Ala Arg Arg Ile Pro Arg Lys Phe Arg Phe Asn 545 550 555 560 Pro Arg Thr Asp Val Gln Val Leu Ala Pro Met His Arg Gly Pro Ala 565 570 575 Gly Ala Gly Ala Leu Asn Gln Leu Leu Gln Glu Ala Ile Thr Pro Ala 580 585 590 Arg Glu Gly Leu Pro Glu Arg Arg Phe Gly Gly Arg Ile Phe Arg Val 595 600 605 Gly Asp Lys Val Thr Gln Ile Arg Asn Asn Tyr Asp Lys Gly Ala Asn 610 615 620 Gly Val Phe Asn Gly Thr Gln Gly Val Val Ser Ala Leu Asp Asn Glu 625 630 635 640 Ala Gln Thr Met Thr Val Arg Thr Asp Glu Asp Glu Asp Ile Asp Tyr 645 650 655 Asp Phe Thr Glu Leu Asp Glu Leu Val His Ala Tyr Ala Val Thr Ile 660 665 670 His Arg Ser Gln Gly Ser Glu Tyr Pro Cys Val Val Ile Pro Leu Thr 675 680 685 Thr Ser Ala Trp Met Met Leu Gln Arg Asn Leu Leu Tyr Thr Ala Val 690 695 700 Thr Arg Ala Lys Lys Val Val Val Leu Val Gly Ser Lys Lys Ala Leu 705 710 715 720 Gly Gln Ala Val Arg Thr Val Gly Ser Gly Arg Arg His Thr Ala Leu 725 730 735 Asp His Arg Leu Arg Arg Gly Gly Thr Gly Ser Arg Pro Ala Ala 740 745 750 25 2310 DNA Saccharopolyspora spinosa CDS (88)..(1077) CDS (1165)..(1992) 25 ggatcctgct tcgtagctcg gtgtgtcatg ccagactgcg cacgcggacc tgcagcgggc 60 cgcgaaatcc cggcgaggaa gggcgcg atg cgg att ctg gtc acc ggc gga gcc 114 Met Arg Ile Leu Val Thr Gly Gly Ala 1 5 ggt ttc atc ggc tcg cac tac gtt cgg cag ttg ctc ggt ggt gcg tac 162 Gly Phe Ile Gly Ser His Tyr Val Arg Gln Leu Leu Gly Gly Ala Tyr 10 15 20 25 ccc gca ttc gcc gac gcc gac gtg gtc gtg ctc gac aag ctc acc tac 210 Pro Ala Phe Ala Asp Ala Asp Val Val Val Leu Asp Lys Leu Thr Tyr 30 35 40 gcc ggc aac gag gcg aac ctg gcg ccg gtc gcg gac aac ccc cgg ctg 258 Ala Gly Asn Glu Ala Asn Leu Ala Pro Val Ala Asp Asn Pro Arg Leu 45 50 55 aag ttc gtc tgc ggc gac atc tgc gac cgc gaa ctg gtt ggc ggc ctg 306 Lys Phe Val Cys Gly Asp Ile Cys Asp Arg Glu Leu Val Gly Gly Leu 60 65 70 atg tcc ggc gtg gac gtg gtg gtg cac ttc gcc gcc gaa acc cac gtc 354 Met Ser Gly Val Asp Val Val Val His Phe Ala Ala Glu Thr His Val 75 80 85 gac cgc tcg atc acc ggc tcg gac gcc ttc gtg atc acc aac gtg gtc 402 Asp Arg Ser Ile Thr Gly Ser Asp Ala Phe Val Ile Thr Asn Val Val 90 95 100 105 ggc acc aac gtg ctg ctg cag gcc gcg ctc gac gcc gag atc ggc aag 450 Gly Thr Asn Val Leu Leu Gln Ala Ala Leu Asp Ala Glu Ile Gly Lys 110 115 120 ttc gtg cac gtt tcc acc gac gag gtc tac ggc tcc atc gag gac ggc 498 Phe Val His Val Ser Thr Asp Glu Val Tyr Gly Ser Ile Glu Asp Gly 125 130 135 tcg tgg ccc gaa gac cac gcg ctg gag ccg aat tcc ccg tac tcg gcg 546 Ser Trp Pro Glu Asp His Ala Leu Glu Pro Asn Ser Pro Tyr Ser Ala 140 145 150 gcg aaa gcg ggc tcg gac ctg ctg gcc cgc gcc tac cac cgc acc cac 594 Ala Lys Ala Gly Ser Asp Leu Leu Ala Arg Ala Tyr His Arg Thr His 155 160 165 gga ctg ccg gtg tgc atc acc cgc tgc tcc aac aac tac ggg ccc tac 642 Gly Leu Pro Val Cys Ile Thr Arg Cys Ser Asn Asn Tyr Gly Pro Tyr 170 175 180 185 cag ttc ccg gag aag gtg ctg ccg ctg ttc atc acg aac ctg atg gac 690 Gln Phe Pro Glu Lys Val Leu Pro Leu Phe Ile Thr Asn Leu Met Asp 190 195 200 ggc agc cag gtg ccg ctc tac ggc gac ggg ctc aac gtg cgg gac tgg 738 Gly Ser Gln Val Pro Leu Tyr Gly Asp Gly Leu Asn Val Arg Asp Trp 205 210 215 ctg cac gtc agc gac cac tgc cgg ggc atc cag ctg gtg gcc gac tcc 786 Leu His Val Ser Asp His Cys Arg Gly Ile Gln Leu Val Ala Asp Ser 220 225 230 ggg cgc gcg ggc gag atc tac aac atc ggc ggc ggc acc gag ctg acc 834 Gly Arg Ala Gly Glu Ile Tyr Asn Ile Gly Gly Gly Thr Glu Leu Thr 235 240 245 aac aac gag ctg acc gag cgg ctg ctg gca gag ctg ggc ctc gac tgg 882 Asn Asn Glu Leu Thr Glu Arg Leu Leu Ala Glu Leu Gly Leu Asp Trp 250 255 260 265 tcg gtg gtg cgg ccg gtc acc gac cgc aag ggc cac gac cgc cgc tac 930 Ser Val Val Arg Pro Val Thr Asp Arg Lys Gly His Asp Arg Arg Tyr 270 275 280 tcg gtg gac cac agc aag atc gtc gag gaa ctg ggg tac gcg ccg cag 978 Ser Val Asp His Ser Lys Ile Val Glu Glu Leu Gly Tyr Ala Pro Gln 285 290 295 gtc gac ttc gag acc ggg ctg cgc gag aca atc cgc tgg tac cag gac 1026 Val Asp Phe Glu Thr Gly Leu Arg Glu Thr Ile Arg Trp Tyr Gln Asp 300 305 310 aac cgg gac tgg tgg gag ccg ctg aag gcc cga tcg gcg gtg gct cga 1074 Asn Arg Asp Trp Trp Glu Pro Leu Lys Ala Arg Ser Ala Val Ala Arg 315 320 325 tga gtcgcctcgc cgtgctggtt gcccggcggc cgcggccagc tgggctcgga 1127 gctggcccgg atcctcgccg cgcggacggg ggcgctg gtg cac cgg ccg ggt tcc 1182 Val His Arg Pro Gly Ser 330 335 ggg gaa ctg gac gtc acc gac gcc gag gag gtc gcc gac gcg ttg ggt 1230 Gly Glu Leu Asp Val Thr Asp Ala Glu Glu Val Ala Asp Ala Leu Gly 340 345 350 tcc ttc gcg gag acg gcg aag gac gcg gag ctg cga ccg gtg gtg atc 1278 Ser Phe Ala Glu Thr Ala Lys Asp Ala Glu Leu Arg Pro Val Val Ile 355 360 365 aac gcc gcg gcg tac acg gcg gtg gac gcg gcc gag tcc gac ccg gac 1326 Asn Ala Ala Ala Tyr Thr Ala Val Asp Ala Ala Glu Ser Asp Pro Asp 370 375 380 cgc gcg gcc cgg atc aac gcc gaa ggc gcg gcc tcg ctg gcg aaa gcg 1374 Arg Ala Ala Arg Ile Asn Ala Glu Gly Ala Ala Ser Leu Ala Lys Ala 385 390 395 tgc cgg agc agc ggt ctg ccc ctg gtg cac gtg tcg acg gat tac gtg 1422 Cys Arg Ser Ser Gly Leu Pro Leu Val His Val Ser Thr Asp Tyr Val 400 405 410 415 ttc ccc cgt gat ggg gcc cgg ccg tac gag ccg acg gac ccg acc ggg 1470 Phe Pro Arg Asp Gly Ala Arg Pro Tyr Glu Pro Thr Asp Pro Thr Gly 420 425 430 ccg cga tcg gtc tac ggg cgc acc aag ctc gaa ggc gaa cgg gcc gtg 1518 Pro Arg Ser Val Tyr Gly Arg Thr Lys Leu Glu Gly Glu Arg Ala Val 435 440 445 ctg gag tcc ggc gcg cgg gcc tgg gtg gtg cgc acg gca tgg gtg tac 1566 Leu Glu Ser Gly Ala Arg Ala Trp Val Val Arg Thr Ala Trp Val Tyr 450 455 460 ggc gcg agc ggc aag aac ttc ctg aaa acg atg atc cgc ctc tcg ggg 1614 Gly Ala Ser Gly Lys Asn Phe Leu Lys Thr Met Ile Arg Leu Ser Gly 465 470 475 gag cgc gac acg ctg tcc gtt gtg gac aat cag atc ggc tcg ccg act 1662 Glu Arg Asp Thr Leu Ser Val Val Asp Asn Gln Ile Gly Ser Pro Thr 480 485 490 495 tgg gcg gcg gac ctg gcg agc ggc ctg ctg gag ctg gcc gaa cgg gtc 1710 Trp Ala Ala Asp Leu Ala Ser Gly Leu Leu Glu Leu Ala Glu Arg Val 500 505 510 gcc gaa cgc cgt gga ccg gag cag aag gtg ctg cac tgc acc aat tcc 1758 Ala Glu Arg Arg Gly Pro Glu Gln Lys Val Leu His Cys Thr Asn Ser 515 520 525 ggc cag gtg acc tgg tac gag ttc gcg cgg gcg atc ttc gcg gaa ttc 1806 Gly Gln Val Thr Trp Tyr Glu Phe Ala Arg Ala Ile Phe Ala Glu Phe 530 535 540 ggc ctg gac gag aac cgc gtc cac ccg tgc acg acg gcg gac ttc ccc 1854 Gly Leu Asp Glu Asn Arg Val His Pro Cys Thr Thr Ala Asp Phe Pro 545 550 555 ctc ccg gcg cac cgc ccg gcc tac tcg gtc ctg tcc gac gtg gcg tgg 1902 Leu Pro Ala His Arg Pro Ala Tyr Ser Val Leu Ser Asp Val Ala Trp 560 565 570 575 cga gag gcg ggc ctg acc ccg atg cgc acc tgg cgg gaa gcc ctg gcg 1950 Arg Glu Ala Gly Leu Thr Pro Met Arg Thr Trp Arg Glu Ala Leu Ala 580 585 590 gcg gcc ttc gag aaa gac ggc gaa acc ctc cga acc cgc tga 1992 Ala Ala Phe Glu Lys Asp Gly Glu Thr Leu Arg Thr Arg 595 400 ccagtcaccc ggagggcgcg agtagccccg gcagggccgt ttcgacgcga tatcggctgg 2052 cgcggtgcgc acaatgggtg tcgccggggc gaggaaggaa ggccaggtgc cccgggggca 2112 tgactgggag cctggcctga tgcctgtccg gggcgttcag cctgcggcga ggcggtatgc 2172 gttcagggtt gcttcggcgc aggttcgcca ggtgaaggct ttagcttggg cacggccctt 2232 ttccgcgtct gggggactgg tcagggcttg gtgcagggct tcgttgaggg ccgtcgggtc 2292 gccgtggggg aagcggat 2310 26 329 PRT Saccharopolyspora spinosa 26 Met Arg Ile Leu Val Thr Gly Gly Ala Gly Phe Ile Gly Ser His Tyr 1 5 10 15 Val Arg Gln Leu Leu Gly Gly Ala Tyr Pro Ala Phe Ala Asp Ala Asp 20 25 30 Val Val Val Leu Asp Lys Leu Thr Tyr Ala Gly Asn Glu Ala Asn Leu 35 40 45 Ala Pro Val Ala Asp Asn Pro Arg Leu Lys Phe Val Cys Gly Asp Ile 50 55 60 Cys Asp Arg Glu Leu Val Gly Gly Leu Met Ser Gly Val Asp Val Val 65 70 75 80 Val His Phe Ala Ala Glu Thr His Val Asp Arg Ser Ile Thr Gly Ser 85 90 95 Asp Ala Phe Val Ile Thr Asn Val Val Gly Thr Asn Val Leu Leu Gln 100 105 110 Ala Ala Leu Asp Ala Glu Ile Gly Lys Phe Val His Val Ser Thr Asp 115 120 125 Glu Val Tyr Gly Ser Ile Glu Asp Gly Ser Trp Pro Glu Asp His Ala 130 135 140 Leu Glu Pro Asn Ser Pro Tyr Ser Ala Ala Lys Ala Gly Ser Asp Leu 145 150 155 160 Leu Ala Arg Ala Tyr His Arg Thr His Gly Leu Pro Val Cys Ile Thr 165 170 175 Arg Cys Ser Asn Asn Tyr Gly Pro Tyr Gln Phe Pro Glu Lys Val Leu 180 185 190 Pro Leu Phe Ile Thr Asn Leu Met Asp Gly Ser Gln Val Pro Leu Tyr 195 200 205 Gly Asp Gly Leu Asn Val Arg Asp Trp Leu His Val Ser Asp His Cys 210 215 220 Arg Gly Ile Gln Leu Val Ala Asp Ser Gly Arg Ala Gly Glu Ile Tyr 225 230 235 240 Asn Ile Gly Gly Gly Thr Glu Leu Thr Asn Asn Glu Leu Thr Glu Arg 245 250 255 Leu Leu Ala Glu Leu Gly Leu Asp Trp Ser Val Val Arg Pro Val Thr 260 265 270 Asp Arg Lys Gly His Asp Arg Arg Tyr Ser Val Asp His Ser Lys Ile 275 280 285 Val Glu Glu Leu Gly Tyr Ala Pro Gln Val Asp Phe Glu Thr Gly Leu 290 295 300 Arg Glu Thr Ile Arg Trp Tyr Gln Asp Asn Arg Asp Trp Trp Glu Pro 305 310 315 320 Leu Lys Ala Arg Ser Ala Val Ala Arg 325 27 275 PRT Saccharopolyspora spinosa 27 Val His Arg Pro Gly Ser Gly Glu Leu Asp Val Thr Asp Ala Glu Glu 1 5 10 15 Val Ala Asp Ala Leu Gly Ser Phe Ala Glu Thr Ala Lys Asp Ala Glu 20 25 30 Leu Arg Pro Val Val Ile Asn Ala Ala Ala Tyr Thr Ala Val Asp Ala 35 40 45 Ala Glu Ser Asp Pro Asp Arg Ala Ala Arg Ile Asn Ala Glu Gly Ala 50 55 60 Ala Ser Leu Ala Lys Ala Cys Arg Ser Ser Gly Leu Pro Leu Val His 65 70 75 80 Val Ser Thr Asp Tyr Val Phe Pro Arg Asp Gly Ala Arg Pro Tyr Glu 85 90 95 Pro Thr Asp Pro Thr Gly Pro Arg Ser Val Tyr Gly Arg Thr Lys Leu 100 105 110 Glu Gly Glu Arg Ala Val Leu Glu Ser Gly Ala Arg Ala Trp Val Val 115 120 125 Arg Thr Ala Trp Val Tyr Gly Ala Ser Gly Lys Asn Phe Leu Lys Thr 130 135 140 Met Ile Arg Leu Ser Gly Glu Arg Asp Thr Leu Ser Val Val Asp Asn 145 150 155 160 Gln Ile Gly Ser Pro Thr Trp Ala Ala Asp Leu Ala Ser Gly Leu Leu 165 170 175 Glu Leu Ala Glu Arg Val Ala Glu Arg Arg Gly Pro Glu Gln Lys Val 180 185 190 Leu His Cys Thr Asn Ser Gly Gln Val Thr Trp Tyr Glu Phe Ala Arg 195 200 205 Ala Ile Phe Ala Glu Phe Gly Leu Asp Glu Asn Arg Val His Pro Cys 210 215 220 Thr Thr Ala Asp Phe Pro Leu Pro Ala His Arg Pro Ala Tyr Ser Val 225 230 235 240 Leu Ser Asp Val Ala Trp Arg Glu Ala Gly Leu Thr Pro Met Arg Thr 245 250 255 Trp Arg Glu Ala Leu Ala Ala Ala Phe Glu Lys Asp Gly Glu Thr Leu 260 265 270 Arg Thr Arg 275 28 1272 DNA Saccharopolyspora spinosa CDS (334)..(1119) 28 aaggccaccg gcaaggtcgt gcagggcatc tcgcaggacg tcgcgaagaa gatctccaag 60 aagatccgcg acgagggccc gaagggcgtt caggcccaga tccagggcga gcagctgcgg 120 gtgtccggca agaagaagga cgacctgcag gccgtgatcc agttgctgaa gtcgagcgac 180 ttcgacgtcg cgctccagtt cgagaatttc cggtaatcca ccgctggagg tatccgggtg 240 aaggggatcg tgctggcggg tggcaacggg acccggctgc atccgctgac gcaggccgtg 300 tccaaacagc tacttccggt gtacgacaag ccg atg atc tac tac ccg ctg tcg 354 Met Ile Tyr Tyr Pro Leu Ser 1 5 gtg ctg atg ctg gcc ggc atc cgg gac gtg ctg ctg atc tcg acc ccg 402 Val Leu Met Leu Ala Gly Ile Arg Asp Val Leu Leu Ile Ser Thr Pro 10 15 20 gcc gac atg ccg ttg ttc cag cgg ctg ctc ggg aac ggg tcg cag ttc 450 Ala Asp Met Pro Leu Phe Gln Arg Leu Leu Gly Asn Gly Ser Gln Phe 25 30 35 ggc att cgg atc gag tac gcc gag cag tcc cag ccc aac ggg cta gcc 498 Gly Ile Arg Ile Glu Tyr Ala Glu Gln Ser Gln Pro Asn Gly Leu Ala 40 45 50 55 gag gcg ttc gtg atc ggt gcc gac ttc gtc ggc gac gac tcg gtg gcg 546 Glu Ala Phe Val Ile Gly Ala Asp Phe Val Gly Asp Asp Ser Val Ala 60 65 70 ttg gtg ctc ggc gac aac atc ttt tac ggg cag ggc ttt tcc ggg atc 594 Leu Val Leu Gly Asp Asn Ile Phe Tyr Gly Gln Gly Phe Ser Gly Ile 75 80 85 ctc cag cag tgc gtc cgg gag ctc gac ggc tgc acg ctg ttc ggc tac 642 Leu Gln Gln Cys Val Arg Glu Leu Asp Gly Cys Thr Leu Phe Gly Tyr 90 95 100 ccg gtc cgc gac ccg cag cgc tac ggc gtc ggt gag gtg gac gac gac 690 Pro Val Arg Asp Pro Gln Arg Tyr Gly Val Gly Glu Val Asp Asp Asp 105 110 115 ggt cgg ctg ttg tcc atc gtg gag aag ccg gag cgg ccg aag tcc aac 738 Gly Arg Leu Leu Ser Ile Val Glu Lys Pro Glu Arg Pro Lys Ser Asn 120 125 130 135 atg gcc atc acc ggc ctg tac ttc tac gac aac gac gtg gtg cgc atc 786 Met Ala Ile Thr Gly Leu Tyr Phe Tyr Asp Asn Asp Val Val Arg Ile 140 145 150 gcc aag ggg ctc acg ccg tcg gcc cgc ggc gag ctg gag atc acc gac 834 Ala Lys Gly Leu Thr Pro Ser Ala Arg Gly Glu Leu Glu Ile Thr Asp 155 160 165 gtc aac ctg gcc tac ctg cag gag ggc cgg gcg cac ctg acc aag ctc 882 Val Asn Leu Ala Tyr Leu Gln Glu Gly Arg Ala His Leu Thr Lys Leu 170 175 180 ggc cgc ggg ttc gcc tgg ctg gac acc ggg acc cac gac tcg cta gtg 930 Gly Arg Gly Phe Ala Trp Leu Asp Thr Gly Thr His Asp Ser Leu Val 185 190 195 gag gcc tcg cag ttc gtg cag gtg ctg gag cac cgg cag ggc gtg cgg 978 Glu Ala Ser Gln Phe Val Gln Val Leu Glu His Arg Gln Gly Val Arg 200 205 210 215 atc gcc tgc ctg gag gag atc ncc ctg cgc atg ggc tac atc tcg gcc 1026 Ile Ala Cys Leu Glu Glu Ile Xaa Leu Arg Met Gly Tyr Ile Ser Ala 220 225 230 gac gac tgt ttc gcg ctg ggc gtg aag ctg gcc aag tcg ggc tac agc 1074 Asp Asp Cys Phe Ala Leu Gly Val Lys Leu Ala Lys Ser Gly Tyr Ser 235 240 245 gag tac gtc atg gac gtc gcc cgc aac tcc ggc gcg cgg ggc tga 1119 Glu Tyr Val Met Asp Val Ala Arg Asn Ser Gly Ala Arg Gly 250 255 260 cccgagctcg tccgatttcc attgaaatcg cggaccgtcg gcgtgtcgta gtccggtgcg 1179 ccgatattcc gggcggcgtc accaggccgg gggtagttgg tggccggcca tgccctccag 1239 gcggcgaaat gcggtcggcc atcggcgggt tgc 1272 29 261 PRT Saccharopolyspora spinosa 29 Met Ile Tyr Tyr Pro Leu Ser Val Leu Met Leu Ala Gly Ile Arg Asp 1 5 10 15 Val Leu Leu Ile Ser Thr Pro Ala Asp Met Pro Leu Phe Gln Arg Leu 20 25 30 Leu Gly Asn Gly Ser Gln Phe Gly Ile Arg Ile Glu Tyr Ala Glu Gln 35 40 45 Ser Gln Pro Asn Gly Leu Ala Glu Ala Phe Val Ile Gly Ala Asp Phe 50 55 60 Val Gly Asp Asp Ser Val Ala Leu Val Leu Gly Asp Asn Ile Phe Tyr 65 70 75 80 Gly Gln Gly Phe Ser Gly Ile Leu Gln Gln Cys Val Arg Glu Leu Asp 85 90 95 Gly Cys Thr Leu Phe Gly Tyr Pro Val Arg Asp Pro Gln Arg Tyr Gly 100 105 110 Val Gly Glu Val Asp Asp Asp Gly Arg Leu Leu Ser Ile Val Glu Lys 115 120 125 Pro Glu Arg Pro Lys Ser Asn Met Ala Ile Thr Gly Leu Tyr Phe Tyr 130 135 140 Asp Asn Asp Val Val Arg Ile Ala Lys Gly Leu Thr Pro Ser Ala Arg 145 150 155 160 Gly Glu Leu Glu Ile Thr Asp Val Asn Leu Ala Tyr Leu Gln Glu Gly 165 170 175 Arg Ala His Leu Thr Lys Leu Gly Arg Gly Phe Ala Trp Leu Asp Thr 180 185 190 Gly Thr His Asp Ser Leu Val Glu Ala Ser Gln Phe Val Gln Val Leu 195 200 205 Glu His Arg Gln Gly Val Arg Ile Ala Cys Leu Glu Glu Ile Xaa Leu 210 215 220 Arg Met Gly Tyr Ile Ser Ala Asp Asp Cys Phe Ala Leu Gly Val Lys 225 230 235 240 Leu Ala Lys Ser Gly Tyr Ser Glu Tyr Val Met Asp Val Ala Arg Asn 245 250 255 Ser Gly Ala Arg Gly 260 30 23 DNA Artificial Sequence Description of Artificial Sequenceprimer 30 ngsgtsggsn ssccaccttc cgg 23 31 33 DNA Artificial Sequence Description of Artificial Sequenceprimer 31 catsangtcg tcytcsansg csacgaacgc gtg 33 32 1165 DNA Artificial Sequence CDS (226)..(834) Description of Artificial SequencepDAB1622 32 gggatcaaca acaacttcac cagcaggttc aacaatttgt caatcccact tggcagtacg 60 cgcgtccttt ttggatcggg attgcggcag tacgtgcacc cggtttcagt gccccatttc 120 gcagtacgta cgtccgtttt gaatatggcg atcaatggct cgcatgaccc atatcaactc 180 cgccccaccg aaccgcattc caaccaacgt cataggcttt cggcc gtg cag gta cgt 237 Val Gln Val Arg 1 cga ctt gac atc acg ggt gca tac gag ttc acc ccg aag gcc ttc ccc 285 Arg Leu Asp Ile Thr Gly Ala Tyr Glu Phe Thr Pro Lys Ala Phe Pro 5 10 15 20 gac cac cgg ggc ctg ttc gtg gcc ccg ttc cag gag gcg gcg ttc atc 333 Asp His Arg Gly Leu Phe Val Ala Pro Phe Gln Glu Ala Ala Phe Ile 25 30 35 gac gcc acg ggg cac ccg ctg cga gtc gcg cag acc aac cac agc gtc 381 Asp Ala Thr Gly His Pro Leu Arg Val Ala Gln Thr Asn His Ser Val 40 45 50 tcg gcg cgc aac gtc atc cgc ggc gtg cac ttc tcg gac gtg ccg ccg 429 Ser Ala Arg Asn Val Ile Arg Gly Val His Phe Ser Asp Val Pro Pro 55 60 65 ggc caa gcg aag tac gtg tac tgc ccg cag ggc gcg ctg ctc gac gtg 477 Gly Gln Ala Lys Tyr Val Tyr Cys Pro Gln Gly Ala Leu Leu Asp Val 70 75 80 gtc atc gac atc cgg gtc ggt tcc ccg acc ttc ggc cgc tgg gag gcg 525 Val Ile Asp Ile Arg Val Gly Ser Pro Thr Phe Gly Arg Trp Glu Ala 85 90 95 100 gtc cgg ctc gac gac acc gag tac cgg gcc gtc tac cta gcc gaa gga 573 Val Arg Leu Asp Asp Thr Glu Tyr Arg Ala Val Tyr Leu Ala Glu Gly 105 110 115 ctc ggg cac gcg ttc gcc gcg ctg acc gac gac acc gtg atg acc tac 621 Leu Gly His Ala Phe Ala Ala Leu Thr Asp Asp Thr Val Met Thr Tyr 120 125 130 ctc tgc tcg acg ccc tac acc ccg ggc gcc gag cac ggc atc gac ccg 669 Leu Cys Ser Thr Pro Tyr Thr Pro Gly Ala Glu His Gly Ile Asp Pro 135 140 145 ttc gac ccg gaa ctc gcg ttg ccg tgg tcc gac ctc gac ggt gaa ccg 717 Phe Asp Pro Glu Leu Ala Leu Pro Trp Ser Asp Leu Asp Gly Glu Pro 150 155 160 gtc ctg tcc gaa aag gac cgg acc gcc ccg agc ctc gcg gaa gcc gcc 765 Val Leu Ser Glu Lys Asp Arg Thr Ala Pro Ser Leu Ala Glu Ala Ala 165 170 175 180 gac aac ggc ctg ctt ccg gac tac gaa aca tgc ctc gcc cac tac gaa 813 Asp Asn Gly Leu Leu Pro Asp Tyr Glu Thr Cys Leu Ala His Tyr Glu 185 190 195 ggc ctg cgc agc ccc ggc tga acggtcaccg caagcggccc ggcttcggcc 864 Gly Leu Arg Ser Pro Gly 200 agaggcgcca ccggataatg ccgagcacct cggccgggcc gagctcccgc gagtccgtcg 924 agccgaagtt gttgtcgccc tcgacgtacc agccatcgcc ctcgcggcgc agcgcgcgct 984 tcaccgacaa ctgccccggg cgctgggccc aacgcaccag cacgacgttt ccccggccgg 1044 gcggaacccc gaagccgcag cagcaccact tcgcgatccc gcagggtggg aaccataaac 1104 ggcccgcgca ccaccaaccg ccgccagggc cagcgcccga gggatttcac atccacctcc 1164 a 1165 33 202 PRT Artificial Sequence 33 Val Gln Val Arg Arg Leu Asp Ile Thr Gly Ala Tyr Glu Phe Thr Pro 1 5 10 15 Lys Ala Phe Pro Asp His Arg Gly Leu Phe Val Ala Pro Phe Gln Glu 20 25 30 Ala Ala Phe Ile Asp Ala Thr Gly His Pro Leu Arg Val Ala Gln Thr 35 40 45 Asn His Ser Val Ser Ala Arg Asn Val Ile Arg Gly Val His Phe Ser 50 55 60 Asp Val Pro Pro Gly Gln Ala Lys Tyr Val Tyr Cys Pro Gln Gly Ala 65 70 75 80 Leu Leu Asp Val Val Ile Asp Ile Arg Val Gly Ser Pro Thr Phe Gly 85 90 95 Arg Trp Glu Ala Val Arg Leu Asp Asp Thr Glu Tyr Arg Ala Val Tyr 100 105 110 Leu Ala Glu Gly Leu Gly His Ala Phe Ala Ala Leu Thr Asp Asp Thr 115 120 125 Val Met Thr Tyr Leu Cys Ser Thr Pro Tyr Thr Pro Gly Ala Glu His 130 135 140 Gly Ile Asp Pro Phe Asp Pro Glu Leu Ala Leu Pro Trp Ser Asp Leu 145 150 155 160 Asp Gly Glu Pro Val Leu Ser Glu Lys Asp Arg Thr Ala Pro Ser Leu 165 170 175 Ala Glu Ala Ala Asp Asn Gly Leu Leu Pro Asp Tyr Glu Thr Cys Leu 180 185 190 Ala His Tyr Glu Gly Leu Arg Ser Pro Gly 195 200 34 28 DNA Artificial Sequence Description of Artificial Sequenceprimer 34 cccgaattcg agctgctgtc aatcaact 28 35 29 DNA Artificial Sequence Description of Artificial Sequenceprimer 35 gggaagcttg ttgaccgtgg cggtttcct 29 36 42 DNA Artificial Sequence Description of Artificial Sequencemutagenic primer 36 ctggttcatt cggccgcctc accggtgggg atggccgcga tc 42 37 42 DNA Artificial Sequence Description of Artificial Sequencemutagenic primer 37 gatcgcggcc atccccaccg gtgaggcggc cgaatgaacc ag 42 38 20 DNA Artificial Sequence Description of Artificial Sequenceflanking primer 38 gctgctcgaa atcgcacgtc 20 39 19 DNA Artificial Sequence Description of Artificial Sequenceflanking primer 39 gcatcgctgg gcagtgagg 19 

We claim:
 1. An isolated DNA molecule comprising a DNA sequence that encodes a spinosyn biosynthetic enzyme, wherein said enzyme is defined by an amino acid sequence selected from the group consisting of SEQ ID NOS 2-5,7-24, 26, 27, 29, 33, or said enzyme is defined by an amino acid selected from SEQ ID NOS 2-5,7-24, 26, 27, 29, 33 in which one or more amino acid substitutions have been made that do not affect the functional properties of the enzyme.
 2. An isolated DNA molecule of claim 1 wherein said DNA sequence is selected from the group of genes consisting of spnA, spnB, spnC, spnD, spnE, spnF, spnG, spnH, spnI, spnJ, spnK, spnL, spnM, spnN, spnO, spnP, spnQ, spnR, spnS, ORFL15, ORFL16, ORFR1, ORFR2, S. spinosa gtt, S. spinosa gdh, S. spinosa epi, and S. spinosa kre, said genes being described by bases 21111-28898, 28916-35374, 35419-44931, 44966-59752, 59803-76569, 20168-20995, 18541-19713, 17749-18501, 16556-17743, 14799-16418, 13592-14785, 12696-13547, 11530-12492, 10436-11434, 8967-10427, 7083-8450, 5363-6751, 4168-5325, 3416-4165, 2024-2791, 1135-1971, 76932-77528, and 77729-79984 of SEQ ID NO: 1, bases 334-1119 of SEQ ID NO:27, bases 88-1077 of SEQ ID NO 24, bases 226-834 of SEQ ID NO 31, and bases 1165-1992 of SEQ ID NO:24.
 3. An isolated DNA molecule comprising a DNA sequence that encodes a spinosyn PKS domain, where said domain is selected from KSi, ATi, ACPi, KS1, AT1, KR1, and ACP1, corresponding, respectively, to amino acid sequences 6-423, 528-853, 895-977, 998-1413, 1525-1858, 2158-2337, and 2432-2513 of SEQ ID NO:2, or said domain is one of said amino acid sequences in which one or more amino acid substitutions have been made that do not affect the functional properties of the domain.
 4. An isolated DNA molecule of claim 3 wherein said DNA sequence is selected from the group consisting of bases 21126-22379, 22692-23669, 23793-24041, 24102-25349, 25683-26684, 27582-28121, and 28404-28649 of SEQ ID NO:1.
 5. An isolated DNA molecule comprising a DNA sequence that encodes a spinosyn PKS domain, where said domain is selected from KS2, AT2, DH2, ER2, KR2, and ACP2, corresponding, respectively, to amino acid sequences 1-424, 536-866, 892-1077, 1338-1683, 1687-1866, and 1955-2034 of SEQ ID NO:3, or said domain is one of said amino acid sequences in which one or more amino acid substitutions have been made that do not affect the functional properties of the domain.
 6. An isolated DNA molecule of claim 5 wherein said DNA sequence is selected from the group consisting of bases 29024-30295, 30629-31621, 31697-32254, 33035-34072, 34082-34621, 34886-35125 of SEQ ID NO:1.
 7. An isolated DNA molecule comprising a DNA sequence that encodes a spinosyn PKS domain, where said domain is selected from KS3, AT3, KR3, ACP3, KS4, AT4, KR4, and ACP4, corresponding, respectively, to amino acid sequences 1-423, 531-280, 1159-1337, 1425-1506, 1529-1952, 2066-2396, 2700-2880, and 2972-3053 of SEQ ID NO:4, or said domain is one of said amino acid sequences in which one or more amino acid substitutions have been made that do not affect the functional properties of the domain.
 8. An isolated DNA molecule of claim 7 wherein said DNA sequence is selected from the group consisting of bases 35518-36786, 37108-38097, 38992-39528, 39790-40035, 40102-41373, 41713-42705, 43615-44157, and 44431-44676 of SEQ ID NO:1.
 9. An isolated DNA molecule comprising a DNA sequence that encodes a spinosyn PKS domain, where said domain is selected from KS5, AT5, DH5, KR5, ACP5, KS6, AT6, KR6, ACP6, KS7, AT7, KR7, and ACP7, corresponding, respectively to amino acid sequences 1-424, 539-866, 893-1078, 1384-1565, 1645-1726, 1748-2172, 2283-2613, 2916-3095, 3188-3269, 3291-3713, 3825-4153, 4344-4638, and 4725-4806 of SEQ ID NO:5, or said domain is one of said amino acid sequences in which one or more amino acid substitutions have been made that do not affect the functional properties of the domain.
 10. An isolated DNA molecule of claim 9 wherein said DNA sequence is selected from the group consisting of bases 45077-46348, 46691-47674, 47753-48310, 49226-49771, 50009-50254, 50318-51592, 51923-52915, 53822-54361, 54638-54883, 54947-56215, 56549-57535, 58106-58990, and 59249-59494 of SEQ ID NO:1.
 11. An isolated DNA molecule comprising a DNA sequence that encodes a spinosyn PKS domain, where said domain is selected from KS8, AT8, DH8, KR8, ACP8, KS9, AT9, DH9, KR9, ACP9, KS10, AT10, DH10, KR10, ACP10, and TE10, corresponding, respectively, to amino acid sequences 1-424, 530-848, 883-1070, 1369-1552, 1648-1726, 1749-2173, 2287-2614, 2640-2800, 3157-3341, 3422-3500, 3534-3948, 4060-4390, 4413-4597, 4900-5078, 5172-5253, and 5302-5555 of SEQ ID NO:6, or said domain is one of said amino acid sequences in which one or more amino acid substitutions have been made that do not affect the functional properties of the domain.
 12. An isolated DNA molecule of claim 11 wherein said DNA sequence is selected from the group consisting of bases 59902-61173, 61489-62445, 62548-63111, 64006-64557, 64843-65079, 65146-66420, 66760-67743, 67819-68301, 69370-69924, 70165-70401, 70471-71745, 72079-73071, 73138-73692, 74599-75135, 75415-75660, and 75805-76566 of SEQ ID NO:1.
 13. An isolated DNA molecule comprising a DNA sequence that encodes a spinosyn PKS module, where said module is selected from the group consisting of amino acid sequences 6-1413 of SEQ ID NO:2, 1525-2513 of SEQ ID NO:2, 1-2034 of SEQ ID NO:3, 1-1506 of SEQ ID NO:4, 1529-3053 of SEQ ID NO:4, 1-1726 of SEQ ID NO:5, 1748-3269 of SEQ ID NO:5, 3291-4806 of SEQ ID NO:5, 1-1726 of SEQ ID NO:5, 1-1726 of SEQ ID NO:6, 1749-3500 of SEQ ID NO:6, and 35434-5555 of SEQ ID NO:6, or said module is one of the said amino acid sequences in which one or more amino acid substitutions have been made that do not affect the functional properties of the domain.
 14. An isolated DNA molecule of claim 13 wherein said DNA sequence is selected from the group consisting of bases 21126-24041, 24102-28649, 29024-35125, 35518-40035, 40102-44676, 45077-50254, 50318-54883, 54947-59494, 59902-65079, 65146-70401, and 70471-76566 of SEQ ID NO:1.
 15. A recombinant DNA vector which comprises a DNA sequence as defined in claim
 1. 16. A host cell transformed with a recombinant vector as claimed in claim
 15. 17. A method of producing spinosyn in increased amounts comprising the steps of: 1) transforming with a recombinant DNA vector or portion thereof a microorganism that produces spinosyn or a spinosyn precurser by means of a biosynthetic pathway, said vector or portion thereof comprising a DNA sequence of claim 1 that codes for the expression of an activity that is rate limiting in said pathway, and 2) culturing said microorganism transformed with said vector under conditions suitable for cell growth and division, expression of said DNA sequence, and production of spinosyn.
 18. A method of claim 17 wherein step 1) comprises transforming said microorganism with a vector or portion thereof comprising a DNA sequence that codes for S. spinosa gtt and S. spinosa gdh.
 19. A transformed spinosyn-producing microorganism having spinosyn biosynthetic genes in its genome wherein at least one of the spinosyn biosynthetic genes, selected from spnA, spnB, spnC, spnD, spnE, spnF, spnG, spnH, spnI, spnJ, spnK, spnL, spnM, spnN, spnO, spnP, spnQ, spnR, spnS, S. spinosa gtt, S. spinosa gdh, S. spinosa epi, and S. spinosa kre, is duplicated.
 20. A transformed spinosyn producing microorganism of claim 19 wherein S. spinosa gtt and S. spinosa gdh are duplicated.
 21. A process for producing a spinosyn compound which comprises cultivating a transformed spinosyn-producing microorganism of claim
 20. 22. A transformed spinosyn producing microorganism of claim 19 wherein S. spinosa gtt, S. spinosa gdh, and S. spinosa kre are duplicated.
 23. A process for producing a spinosyn compound which comprises cultivating a transformed spinosyn-producing microorganism of claim
 22. 24. A process for producing a spinosyn compound which comprises cultivating a transformed spinosyn-producing microorganism of claim
 19. 25. A transformed spinosyn-producing microorganism having spinosyn biosynthetic genes in its genome, wherein at least one of said genes has been disrupted by recombination with an internal fragment of that gene, the rest of said genes being operational to produce a spinosyn other than the one that would be produced if the disrupted gene were operational.
 26. A process for producing a spinosyn compound which comprises cultivating a transformed spinosyn-producing microorganism of claim
 25. 27. A transformed spinosyn-producing microorganism having operational spinosyn biosynthetic genes including multiple PKS modules in its genome, wherein said genes a) include at least one operational PKS module more or at least one less than is present in SEQ ID NO:1; or b) include a PKS module that differs from the corresponding module described in SEQ ID NO:1 by the deletion, inactivation, or addition of a KR, DH or ER domain, or by the substitution of an AT domain that specifies a different carboxylic acid.
 28. A process for producing a spinosyn which comprises cultivating a transformed spinosyn-producing microorganism of claim
 27. 29. A process for isolating a macrolide biosynthetic gene which comprises creating a genomic library of a macrolide producing microorganism, and using a labeled fragment of SEQ ID NO:1, SEQ ID NO:25, SEQ ID NO:28, or SEQ ID NO:32 that is at least 20 bases long as a hybridization probe.
 30. A process of claim 29 wherein the microorganism is a spinosyn producing microorganism. 